{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5848284004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5073312004,"location":{"name":"Remote"},"metadata":null,"id":5848284004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"128","title":"Associate Director, Biostatistics","company_name":"Definium Therapeutics","first_published":"2026-04-03T11:59:33-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;As an Associate Director, Biostatistics this person will provide statistical support for pipeline compounds’ clinical development, regulatory filing, and commercialization. Reporting to Vice President, Head of Biometrics and Data Science, the successful candidate will serve as the biostatistician for assigned clinical trials to provide statistical leadership from trial design, data analysis, to results interpretation and dissemination. This role will also provide statistical support to regulatory filing dossier preparation. As a hands-on biostatistician, this individual will be responsible for all statistical deliverables for the assigned projects in collaboration with members Biometrics team and in multi-functional project teams. Working closely with Definium Statistical Programming group, this individual will oversee the deliverables from statistical vendors to ensure high quality and meeting timeline. Additionally, the responsibilities of this individual include performing statistical analyses on trial data using SAS programs and partnering with the Clinical Data Management group to support data cleaning activities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as Study Biostatistician for assigned clinical trials to provide statistical support from design, analysis to reporting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the biostatistician conducting integrated data analyses to support regulatory filing dossier preparation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross-functional experts on clinical trial designs and make contributions to determination of objectives, endpoints and sample size\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author statistical methods section in the protocol and review the protocol throughout\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Make certain the accuracy of randomization algorithm and contribute to eCRF design to ensure that study objectives, data analysis and data collection are aligned\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with statistical vendors and internal Statistical Programming team to deliver study results or integrated analyses with quality and speed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide statistical input to any form of data reporting or external dissemination, including clinical study report, regulatory communication and publication\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct data analyses as needed by using own SAS programs in collaboration with internal Statistical Programming team\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications and Skills:\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A PhD degree in Statistics, Biostatistics or relevant fields with at least 7 years’ working experience, or a Master’s degree in Statistics, Biostatistics or relevant fields with at least 10 years’ working experience, in pharmaceutical or biotechnology companies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid statistical knowledge and experience in clinical trial design (early to late phase), data analysis, and reporting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Rich experience in authoring study SAP and TFL shells and driving the review process to achieve consensus among review functions to deliver the final versions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience in managing statistical vendors to implement SAP and deliver study results with quality and speed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid knowledge and extensive experience of using statistical computational languages, such as SAS, to perform data analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of regulatory guidance relevant to clinical trials from design to analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated capacity of collaboration with Clinical Development, Clinical Operations, Regulatory Affairs, Data Science and other relevant functions to deliver common goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational and project management skills; demonstrated interest in continued learning and growing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented and hold high standards of excellence for their work products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deliver and communicate effectively in the work-from-home environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal skills and is a good team player\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Experience \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in CNS drug development from clinical trials design to data analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in regulatory filing from integrated data analysis planning and execution to submission dossier preparation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $183,656.00 - $208,950.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4096939004,"name":"36 - Biometrics \u0026 Data Science","child_ids":[],"parent_id":4037866004}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5977186004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5144887004,"location":{"name":"Remote"},"metadata":null,"id":5977186004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"140","title":"Associate Director, Clinical Development","company_name":"Definium Therapeutics","first_published":"2026-04-20T16:59:57-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;The Associate Director, Clinical Development plays a key role in the design and execution of ongoing and new clinical development studies. This position serves as the clinical science representative on one or more U.S. and/or global clinical studies and contributes to the delivery of high‑quality clinical data to support registration and launch. The role partners cross‑functionally with Clinical Operations, Clinical Pharmacology, Regulatory Affairs, Early Development, Medical Affairs, Commercial, and external vendors.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as a responsible member and clinical science representative on global development teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross‑functional partners to provide clinical development expertise in support of study execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide therapy‑area medical and scientific expertise in the evaluation and presentation of clinical trial data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Write and edit clinical protocols, clinical study reports, manuscripts, and other study‑related documents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the quality, coordination, and timeliness of clinical sections of regulatory deliverables (e.g., INDs, Investigator Brochures, CTAs, ISS/ISE, clinical expert reports) in partnership with Regulatory Affairs and Project Management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and monitor patient‑level and study‑level data, including participation in blinded data review and use of data science approaches as applicable\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with statisticians and programmers on statistical analysis plans and interpretation of clinical data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with Medical Writing to support abstracts, manuscripts, and presentations for external scientific meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as the clinical science lead to CROs and external vendors, with appropriate oversight from senior leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to a culture of innovation, collaboration, and continuous improvement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform additional responsibilities as assigned by leadership\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Doctoral degree required (PhD, MD, PharmD, PsyD, MA, LCSW)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 3 years of clinical development experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in CNS development (psychiatry or neurology) strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of late‑stage clinical development and regulatory processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in data review, analysis, and regulatory writing (e.g., IND and CTD sections)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to work collaboratively across functions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Other Skills \u0026amp;amp; Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Managerial experience a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to anticipate challenges and propose thoughtful, evidence‑based solutions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to travel as required, including international travel (typically 10–20%, may reach higher during peak periods)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $169,814.00 - $192,241.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4037866004,"name":"25 - Clinical Development","child_ids":[4096939004,4103605004],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/6010260004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5160680004,"location":{"name":"Remote"},"metadata":null,"id":6010260004,"updated_at":"2026-06-02T16:12:30-04:00","requisition_id":"155","title":"Associate Director, Medical Marketing","company_name":"Definium Therapeutics","first_published":"2026-06-02T10:51:03-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;The Associate Director, Medical Marketing will support the development and execution of strategic medical marketing initiatives to drive the successful commercial launch of DT120, working closely with Medical Affairs, Regulatory, Commercial, Clinical Development, and cross-functional teams to align with corporate goals. This role will help shape scientific engagement strategy through KOL development, advisory boards, congress activities, and evidence communication initiatives, while ensuring all activities meet applicable regulatory and compliance standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute medical marketing initiatives that support the scientific positioning and successful commercialization of DT120\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead KOL engagement strategy, including identification, segmentation, relationship development, and ongoing engagement planning\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage advisory board planning and execution, including objectives, attendee selection, content development, logistics, and insight capture\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support medical congress strategy and execution, including sponsorships, exhibits, symposia, scientific communications, and stakeholder engagement activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Medical Affairs, Clinical Development, Commercial, and Regulatory teams to align scientific engagement activities with broader organizational objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct external agency partners and vendors supporting congresses, advisory boards, speaker programs, and scientific communications initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Gather and synthesize insights from KOL interactions, advisory boards, congresses, and market intelligence to inform brand and evidence-generation strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development of scientific communication materials and engagement initiatives that strengthen awareness, credibility, and launch readiness\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in Life Sciences, Marketing, Business, Communications, or related discipline; advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 8 years in the pharmaceutical, biotech, or healthcare industry, with experience in medical marketing, medical affairs operations, scientific communications, or commercial launch support\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of pharmaceutical regulations governing scientific exchange, promotional activities, and healthcare professional engagement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing KOL engagement programs, advisory boards, and medical congress activities required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to lead initiatives and influence cross-functional teams in a matrixed environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in analyzing scientific, clinical, and market insights to inform strategic decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled in cross-functional collaboration; intellectually curious, solutions-oriented, and effective at communicating and socializing strategic recommendations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Launch experience in the U.S. pharmaceutical market preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting scientific communications, congress planning, speaker programs, or publication-related activities preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in CNS / psychiatry, specialty pharmaceutical, or complex treatment categories preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with REMS products or novel treatment delivery models preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to synthesize complex clinical and market data into actionable strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong presentation skills and ability to influence senior, cross-functional, KOL, and agency stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel as required; average 20–30%, with higher travel during congress and launch periods\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $170,000.00-197,911.00, with compensation determined based on several factors including skill set, years of experience, and geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4037872004,"name":"11 - Marketing","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/6002558004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5157543004,"location":{"name":"Remote"},"metadata":null,"id":6002558004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"152","title":"Director, Biostatistics","company_name":"Definium Therapeutics","first_published":"2026-05-21T11:04:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;As Director, Biostatistics, this role will provide statistical support for clinical development of Definium’s pipeline compounds, regulatory filing, and commercialization effort. Reporting to Vice President, Head of Biometrics and Data Science, this role will serve as the lead biostatistician for the assigned clinical programs and/or clinical studies, providing statistical leadership from clinical trial design, data analysis - covering planning and execution - to results interpretation and dissemination. This role will be hands-on while offering statistical and strategic input to all clinical activities where statistical input can make a difference or is requested. A key responsibility of this role will be ensuring that the deliverables from our statistical vendors are of high quality and meet deadlines, in close collaboration with the Definium Statistical Programming group and multi-functional teams. Additionally, the role will perform statistical analyses using own SAS programs as needed, and support data cleaning activities in collaboration with the Clinical Data Management group and other functions within Clinical Development organization. \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide statistical input to the creation of clinical development plan for the assigned compound(s)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross-functional experts on clinical trial designs and make contributions to determination of objective, endpoints and sample size\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Play as an integral part of a protocol development team by authoring statistical methods section and reviewing the protocol throughout\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure the accuracy of randomization algorithm and contribute to eCRF design to ensure data collection’s alignment with study objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be the primary owner of study statistical analysis plan (SAP) for the assigned clinical trials alongside the shells for table/figures/listing (TFL) that present the analytic results and reflect the analysis intent specified in the SAP\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hold the primary responsibility of working with statistical vendors to implement the SAP and deliver study results with quality and speed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hold the primary responsibility of managing statistical vendors to deliver other data analyses as needed (e.g., DMC support, interim analysis)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide statistical input to any form of data reporting or external dissemination, including clinical study report, regulatory communication and publication\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct data analyses as needed by using own SAS programs in collaboration with Statistical Program group for validation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the development of Biometrics’ SOPs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications and Skills:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A PhD degree in Statistics or Biostatistics with at least 10 years’ working experience in pharmaceutical or biotechnology companies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid statistical knowledge and experience in clinical trial design from early to late phase, data analysis and reporting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong track record using statistical methods to solve real problems emerged in clinical trials and resulted in right decision-making and/or compound advancement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Rich experience is authoring study SAP and TFL shells and driving the review process to achieve consensus among review functions to deliver the final versions of high quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience in managing statistical vendors to implement SAP and deliver study results with quality and speed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid knowledge and extensive experience of using statistical computational languages, such as SAS, to perform data analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of regulatory guidance relevant to clinical trials from design to analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated capacity of collaboration with Clinical Development, Clinical Operations, Regulatory Affairs, Data Science and other relevant functions to deliver common goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational and project management skills; demonstrated interests of continued learning and growing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented and hold high standards of excellence for own work products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deliver and communicate effectively in the work-from-home environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal skills and is a good team player\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $224,643.00 - $249,312.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;","departments":[{"id":4096939004,"name":"36 - Biometrics \u0026 Data Science","child_ids":[],"parent_id":4037866004}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5984722004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5148626004,"location":{"name":"Remote"},"metadata":null,"id":5984722004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"142","title":"Director, HEOR","company_name":"Definium Therapeutics","first_published":"2026-04-29T13:06:00-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;We are seeking a Director of Health Economics \u0026amp;amp; Outcomes Research (HEOR) to support the development and implementation of innovative and strategically focused value evidence generation activities supporting the clinical development, commercialization, and access of Definium products in therapeutic area of brain health disorders. The candidate is responsible for designing and developing research projects, conducting analysis, reporting and publication of HEOR studies, and providing methodologic input to the clinical development needs (where warranted) throughout the product lifecycle. Experience in executing real-world and prospective studies and patient-centered outcomes assessments (PCOA) is preferred.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;The role will report to the Senior Director, HEOR. While the focus is for the U.S. market, the candidate may be called upon to work across different time zones at times. The successful candidate is driven, self-sufficient, curious, collaborative, with a bold ambition to contribute to ground-breaking drug development with potential to transform brain health diseases with very high unmet medical need. She/he is a generous collaborator with innovative approaches, and a willingness to learn new concepts while working in a fast-growing, dynamic environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Leads the design, implementation and management of HEOR studies from concept development through publication. HEOR studies may include, but are not limited to, prospective research studies, patient interviews, and payer-focused tools (i.e. dossier, external facing assets)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help identify evidence gaps and needs from regulatory, reimbursement and patient perspectives, resolve these challenges and translate strategic objectives into the HEOR / Real-World Evidence (RWE) plan\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Directs the generation of necessary evidence to demonstrate product differentiation and values, and / or to support clinical development, regulatory needs through RWE and epidemiology studies in a timely and strategic manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with other functions in cultivating strong internal partnerships, including research and development strategy, epidemiology, regulatory, policy, market access and medical affairs on the development on programs that support broad access and value\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support proactive engagement with payer advisors and KOL stakeholders including generating strategic insights on endpoints, PCOA, and trial design. Identify relevant PCOA endpoints and provide input to the clinical development plan\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Psychometric validation of patient-reported outcomes and instruments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help develop protocols for RWE (prospective and retrospective) analyses, PROs, surveys/patient interviews and provide innovative solutions on RWE for use as a synthetic/historical or concurrent control, including expertise on methodological considerations to account for confounding, missing variable, temporal or other biases and/or methodological challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in evidence synthesis (in conducting systematic literature review, indirect treatment comparisons, gap analyses for effectiveness, meta-analysis)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Publications and other functions on development of real-world evidence publications for congresses and peer-reviewed journals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide project and vendor management support, including request for proposal, statement of work, vendor selection, legal \u0026amp;amp; compliance issues, and budget tracking\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain strong, collaborative relationships with the broader Definium organization and with external experts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help support and manage deliverables such as value dossiers, reimbursement dossiers, reimbursement landscape analyses, consultant driven research projects\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure that deliverables are accomplished on time and within budget\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree (MS, MPH, MD, PhD, PharmD) in health economics, epidemiology, health services research\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 5-7 years’ experience in HEOR in an industry setting, preferably in psychiatry or neuroscience related therapeutic areas\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent knowledge of market access environment and health technology assessment process in the U.S. and key European markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience in designing HEOR protocol elements both within phase III / non-interventional study programs and phase IV/post-marketing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous new product launch experience a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated business and scientific acumen\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent analytic and problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to understand and effectively communicate scientific information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently, proven oral and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work effectively in a fast-paced, collaborative environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Aptitude to closely collaborate and bond with an entirely remote team, willing to travel on a regular basis for in-person team meetings (projected ~25% – 30% travel)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $227,109.00 - $255,000.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;","departments":[{"id":4118474004,"name":"26 - VEOR","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/6010249004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5160677004,"location":{"name":"Remote"},"metadata":null,"id":6010249004,"updated_at":"2026-06-02T16:04:14-04:00","requisition_id":"154","title":"Director, Patient \u0026 Digital Marketing","company_name":"Definium Therapeutics","first_published":"2026-06-01T15:49:45-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;The Director, Patient \u0026amp;amp; Digital Marketing will support the development and execution of strategic patient / consumer marketing initiatives to drive the successful commercial launch of DT120, working closely with regulatory, medical, market access, and cross-functional commercial teams to align with corporate goals. This role will help shape patient engagement strategy across disease education, branded promotion, and omnichannel digital activation, while ensuring all initiatives meet stringent regulatory standards (e.g., FDA).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute patient / consumer marketing strategies and annual brand plans to support the successful launch and commercialization of DT120\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage key patient marketing initiatives across the product lifecycle, including pre-launch planning, audience segmentation, campaign execution, performance measurement, and optimization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive digital patient engagement strategy, including branded and unbranded web experiences, CRM, social media, search, and other non-personal promotional initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee the promotional review process (MLR/PRC) to ensure all patient-facing marketing materials are compliant with regulatory requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Medical Affairs, Market Access, Patient Services, Sales, and cross-functional commercial teams to align patient engagement strategies with broader business objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct external agency partners across creative, digital, media, analytics, and market research to deliver high-impact, ROI-driven initiatives within budget\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate patient, caregiver, and market insights into actionable strategies that strengthen engagement, differentiation, and launch readiness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support patient advocacy, congress, and community engagement initiatives that enhance awareness, education, and brand presence\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Life Sciences, Marketing, Business, Communications, or related discipline; advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 10 years in the pharmaceutical, biotech, or healthcare industry, with experience in patient / consumer marketing, digital marketing, and product launch support\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of pharmaceutical regulations governing patient / consumer promotion and digital communications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with branded and unbranded patient / consumer marketing required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to lead initiatives and influence cross-functional teams in a matrixed environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in analyzing market trends, competitive intelligence, patient insights, and campaign performance to inform strategic decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled in cross-functional collaboration; intellectually curious, solutions-oriented, and effective at communicating and socializing strategic recommendations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Launch experience in the U.S. pharmaceutical market required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with digital engagement platforms, CRM, web strategy, social media, and non-personal promotion required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in CNS / psychiatry, specialty pharmaceutical, or complex treatment categories preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with REMS products or novel treatment delivery models preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to synthesize complex clinical, market, and customer data into actionable strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong presentation skills and ability to influence senior, cross-functional, and agency stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel as required; average 10–20%, with higher travel during key launch periods\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $204,944.00-$225,246.00, with compensation determined based on several factors including skill set, years of experience, and geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4037872004,"name":"11 - Marketing","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5990864004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5151888004,"location":{"name":"Remote"},"metadata":null,"id":5990864004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"145","title":"Director, Product Communications","company_name":"Definium Therapeutics","first_published":"2026-05-11T09:37:31-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;We are seeking a seasoned, dynamic Director, Product Communications to lead strategic communications for the company’s late-stage pipeline, including Phase 3 data readouts, potential regulatory filings, and future launch readiness. This role will be central to shaping the external and internal narrative around Definium’s scientific rigor and innovation, stewarding corporate and product reputation through critical clinical milestones, and helping prepare the market for a potential first-in-class launch.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This individual will report into the VP of Corporate Communications, and will work in close partnership with Commercial, Medical Affairs, Investor Relations, Human Resources, Patient Advocacy, Government Affairs, and other cross-functional leaders to develop clear, compliant, and high-impact messaging and programming across earned, owned, social/digital, and shared channels. The goal is to ensure Definium’s story is communicated with consistency, credibility, and relevance to key stakeholders, including employees, patients, healthcare providers, investors, and payers.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate is an experienced communications professional with deep pharmaceutical experience who can operate strategically and execute flawlessly in a fast-paced, high-visibility, environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Responsibilities:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the development and execution of integrated communications programs that elevate awareness of product differentiation and their potential to address unmet medical needs in support of company goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the communications lead for our commercial product teams and participate in regular team planning meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish collaborative working relationships with R\u0026amp;amp;D, medical affairs, regulatory, government affairs, and brand teams to develop communications plans that shape differentiated messaging across audiences that redefine a new era in psychedelics and psychiatric care\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct multiplatform, integrated PESO (paid, earned, social, owned) communications campaigns\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and deploy media relations plans; work with and maintain relationships with journalists\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reflecting the increasingly social/digital way that key audiences get their information, a predominant focus will be on the strategic design and implementation of sophisticated, highly targeted social/digital efforts designed to educate, raise awareness, and shape the market ahead of potential launch\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support KPI and measurement framework development, and provide regular readouts/metrics tracking with recommendations for optimization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead reputation and issues preparedness planning, including scenario planning, Q\u0026amp;amp;A development, and leadership briefings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Medical Affairs and Clinical Development to ensure accurate translation of complex scientific information into clear, compliant, targeted communications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop engaging employee communications that inform, align, and excite colleagues about our pipeline and products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee materials through Definium’s internal review systems, ensuring all content meets regulatory, legal, and business standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent function on integrated teams and proactively contribute to decision-making with business partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage PR agency, ensuring alignment between internal decisions and agency work product, while ensuring delivery of high-quality, strategically aligned work on time and on budget\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help ensure Definium remains on the cutting edge by incorporating the latest technology (e.g., AI) and data into planning and measurement efforts\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Qualifications:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree with a minimum of 10 years in the pharmaceutical or biotech industry, with experience in product communications, ideally with CNS, psychiatry, or neurology experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Significant experience in clinical data communications, with a proven ability to synthesize complex data into actionable strategies and work across functions to secure alignment and approvals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous in-house and agency experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of the US healthcare landscape, including regulatory policy and market access, and the fast-paced media environment across earned and digital/social platforms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to set strategy and long-range plans while driving outcomes in a hands-on manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong executive presence with demonstrated experience advising senior leaders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written, verbal, and interpersonal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing agencies, budgets, and cross‑functional alignment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexibility and agility to navigate dynamic, fast-paced environments; ability to adapt with evolving business needs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative team player with an enterprise mindset who can work effectively in cross-functional teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently motivated, detail-oriented, and good problem-solving ability\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Up to 20% of travel may be required based upon business needs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $192,904.00 - $226,600.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4083007004,"name":"19 - Corporate Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5848374004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5073364004,"location":{"name":"Remote"},"metadata":null,"id":5848374004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"130","title":"Director, Statistical Programming","company_name":"Definium Therapeutics","first_published":"2026-04-03T13:28:13-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;As Director, Statistical Programming, this person will provide statistical programming leadership to support analysis and reporting for assigned clinical programs, as well as to support pipeline compounds’ regulatory filing and commercialization. Reporting to Vice President, Head of Biometrics and Data Science, this person will lead a group of Statistical Programmers to deliver while also being hands-on. This individual will work closely with biostatisticians for data analysis, vendor supervision and provide programming leadership to support Definium’s integrated data analyses and integrated data packages for regulatory filing. This role will be an integral part of multi-functional project team to provide strategic and technical input as one of the subject-matter-experts. \u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage a group of statistical programmers to provide programming support for assigned projects from datasets creation (or validation) to data analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Join the regulatory filing team and serve as the lead statistical programmer to support integrated data analyses and ensure all data requirements are met for regulatory filing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for delivering high quality analysis datasets (SDTM and ADaM) from meeting CDISC standards to ensuring accuracy of all derived variables either for assigned clinical trials or for integrated databases\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for delivering high quality integrated databases to support integrated safety and efficacy analyses\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for high quality DEFINE packages for SDTM and ADaM either for assigned clinical trials or for integrated databases\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with biostatisticians to manage vendor’s deliverables from quality to timeline\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform statistical data analysis using own SAS programs as needed to support decision making, regulatory communication or drug product commercialization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform independent validation using own SAS programs to ensure accuracy of statistical vendor’s deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in developing necessary SOPs or processes governing statistical programing activities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications and Skills\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Master\u0026#39;s Degree in Biostatistics, Statistics, Computer Science or other relevant fields with at least 15 years of experience in using statistical programming to support clinical trial data analysis in pharmaceutical, biotech or CRO environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Rich experience of building and leading statistical programming groups to deliver across programs often with competing priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding about data standards with solid knowledge in creating DEFINE packages to support regulatory filing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in statistical computational software such as SAS, including complicated data steps, SAS macro languages, and commonly used analysis procedures (e.g., PROC Freq, PROC REPORT, PROC GLM, and PROC MIXED)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience in managing statistical vendors to deliver with quality and speed and within the budget\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills, project and resources management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented and hold high standards of excellence for Statistical Programming group’s deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deliver and communicate effectively in the work-from-home environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong track record of problem solving with demonstrated interests of continued learning and growing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal skills and is a good team player\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Experience \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in providing statistical programming support for CNS clinical trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in providing statistical programming support for regulatory filing\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $216,951.00 - $241,497.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;","departments":[{"id":4096939004,"name":"36 - Biometrics \u0026 Data Science","child_ids":[],"parent_id":4037866004}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/6001294004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5157054004,"location":{"name":"Hybrid (San Diego, CA)"},"metadata":null,"id":6001294004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"150","title":"End User Computing Engineer","company_name":"Definium Therapeutics","first_published":"2026-05-28T15:32:31-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Reporting to the Sr. Director of Information Technology, the End-User Computing (EUC) Engineer will be responsible for providing primary operational support for end-user hardware and software for a fully remote and geographically distributed company with a growing physical presence in Raleigh/Durham, \u0026lt;strong\u0026gt;San Diego\u0026lt;/strong\u0026gt; and Philadelphia. The prospective candidate will provide level 1 and 2 support for the enterprise and collaborate with senior members of IT on resolution of next-level support issues. The candidate will drive and participate in design, architecture, engineering, implementation, and operations of Definium global SaaS IT and business application portfolio to establish and maintain core operational, compliance, security, privacy, and other KPIs and standards. He/she will have a passion for problem solving, thrives in a diverse global organization, provides an excellent end-user experience, explores innovative technologies, and is driven to seek continuous improvement.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide operational support for remote staff. This will include hardware and software issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create, update, triage, and close support tickets in the Definium ITSM to ensure a thorough documentation of requests and incidents, end-user communication, root cause analysis and resolution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;IT lead for all new and departing employee responsibilities. Ensure compliance with all on-boarding and off-boarding policies and procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate the hardware lifecycle for remote employees from procurement, configuration, collection, and retirement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide primary/secondary system administration to IT systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with IT MSPs and professional service providers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in identifying, evaluating, justifying, and deploying, new products, technologies, systems, services, and workflows\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently perform actions under departmental change control procedures with minimal oversight or assistance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance for technology projects and processes including Sarbanes Oxley (SOX), 21 CFR Part 11, cGxP, and GDPR\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and review standard operating procedures and knowledge-based articles for the maintenance and operation of software applications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure that best practices for the service and support of technology products are documented and followed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stay up to date on industry trends and best practices\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum bachelor’s degree or equivalent work experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years of Tier I operational support experience, preferably within a regulated life sciences environment that has a remote or hybrid workforce\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years supporting macOS and Windows laptops via MDM\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years supporting Identity platforms [OKTA or Entra/AzureAD]\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years supporting SaaS applications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience administering Co-Pilot, M365, SharePoint, Powershell, Cisco Umbrella, CrowdStrike, CheckPoint, M365, Slack, Zoom, DocuSign, FreshService, Intune, Kandji, Apple Business Manager, Adobe, and OKTA\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent vendor management and negotiation skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong remote triaging skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience managing SharePoint sites and M365 permissions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;SOX and/or 21 CFR Part 11 experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting multiple operating systems (Windows 11, iOS, and MacOS)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;ITIL certification preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $100,932.00 - 123,380.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4037862004,"name":"16 - IT/Facility","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5848310004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5073331004,"location":{"name":"Remote"},"metadata":null,"id":5848310004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"129","title":"Executive Director, Commercial Supply Chain","company_name":"Definium Therapeutics","first_published":"2026-04-03T11:58:26-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree (or equivalent) in science or business with 15+ years of relevant experience in pharmaceutical supply chain, including specialty product launches\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in strategic global supply chain, commercial manufacturing, and supplier relationship management in a virtual environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience forming, developing, and leading a pharmaceutical commercial supply chain function ideally in a virtual environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Significant experience leading and influencing raw material, small molecule drug substance, bulk drug product, and final packaging suppliers at multiple levels of the organization up to site leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record and expertise in leading successful launch and supply of specialty pharmaceutical products, ideally for Schedule II-V controlled drugs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience establishing systems used to support commercial products in a first launch environment, including inventory and supply planning software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience leading the serialization implementation that is Drug Supply Chain Security Act (DSCSA) compliant\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive understanding of pharmaceutical development, manufacturing, packaging and labeling, serialization, and distribution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of channel strategy design and implementation, including both hub and wholesaler models\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working understanding of current good manufacturing practices (cGMPs) and current good distribution practices (cGDPs)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong initiative, accountability, independence and willingness to take ownership and drive projects to completion\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to effectively build relationships to partner both externally and internally, including with Quality, Trade and Distribution, Pharmaceutical Development, Compliance, and Program Management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capability and vision to think strategically, coupled with the drive to implement, collaborate, and contribute across disciplines\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;The Executive Director of Commercial Supply Chain Strategy will be accountable for establishing the global commercial supply chain function, commercial supplier oversight, and deliverables supporting launch and on-going supply for Definium products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This role will provide leadership and vision in establishing the Commercial Supply Chain function by leveraging processes, building capability, meeting commercial supply chain requirements deliverables, and driving supply chain maturity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain end-to-end global supply chain strategy and supply network from drug substance through to finished drug product\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee management of commercial contract manufacturers suppliers and identify opportunities for efficiencies and cost reduction\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work directly with external manufacturers and packaging organizations stakeholders to establish commercial supply agreements, meet commercial supply demand, and plan for future forecast\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Trade and Distribution to select and oversee third party logistics providers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead end to end value chain planning - inventory management across raw materials, drug substance, drug products and finished goods\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement and integrate serialization solution through supply and distribution network that meets most recent DSCSA compliance requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and optimize processes and systems (i.e. ERP) by working directly with commercial, pharmaceutical development, quality, and finance to ensure short and long-term manufacturing supply needs are met\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $238,000.00 - $310,000.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4037871004,"name":"50 - Pharm Development","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/6014056004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5162197004,"location":{"name":"Hybrid"},"metadata":null,"id":6014056004,"updated_at":"2026-06-04T11:19:31-04:00","requisition_id":"156","title":"IT System Business Partner - Commercial and Medical","company_name":"Definium Therapeutics","first_published":"2026-06-04T11:08:43-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the Vice President of Information Technology, IT Systems Business Partner – Commercial and Medical serve as the primary strategic liaison between IT and Commercial (e.g. Sales, Marketing, and Market Access), Medical Affairs, and Health Economics and Outcomes Research (HEOR). This role ensures technology solutions are tightly aligned with commercial and medical strategy, regulatory obligations, and business objectives. The ideal candidate combines strong business acumen with IT administration and delivery experience, acting as a trusted advisor to business leaders while translating needs into scalable, secure, and compliant technology solutions.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Act as the primary IT point of contact for Commercial and Medical Affairs leadership, developing strong, trust‑based partnerships\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Understand the Commercial and Medical Affairs strategy, business goals, and operational challenges, aligning business objectives to clear, prioritized IT initiatives and requirements\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Support systems and new product introduction by providing technical expertise, system administration, problem solving, and strategies for risk mitigation\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Support the overall governance and lifecycle management of commercial and Medical Affairs systems and platforms. (e.g., Veeva Vault CRM, Open Data, Link, Approved Email)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Lead requirements gathering, documentation, and testing for commercial and Medical Affairs platforms. Ensure configuration, enhancement, and expansion of the systems aligns with broader organizational data standards, information security practices, and regulatory needs\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Work closely with IT and Legal to ensure data protection controls such as segmentation and access boundaries are designed, implemented, and consistently enforced in alignment with regulatory requirement\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Ensure alignment between business demand and IT capacity and prioritization\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Provide oversight and system administration across SaaS platforms supporting Commercial operations and Medical Affairs. (e.g., CRM, field enablement, analytics, content management)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Ensure solutions are scalable, user‑centric, and aligned with enterprise architecture standards\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Monitor delivery risks, dependencies, and change impacts; escalate as appropriate Serve as a clear communicator between technical and non‑technical stakeholders\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Drive change management, user adoption, and ongoing optimization of deployed solutions.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;· Bachelor’s degree in Information Systems, Business, or a related field (or equivalent experience)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;· 7+ years of experience in IT, business systems, or technology business partnering roles supporting Commercial functions (Sales, Marketing, or adjacent teams) within a regulated life sciences environment\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;· 5+ experience building and supporting CRM, Medical Affairs and Commercial enablement platforms. Veeva Commercial suite, Data Bricks, Snowflake, SQL experience strongly preferred\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;· Veeva certifications are strongly preferred\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;· Familiarity with regulatory frameworks (GxP, HIPAA, GDPR) and data integrity principles\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;· Exceptional communication and stakeholder management skills\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;· Proven ability to influence without authority and manage senior stakeholder relationships\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is\u0026amp;nbsp;$161,240 - $192,400 Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4037862004,"name":"16 - IT/Facility","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5973863004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5144266004,"location":{"name":"Remote"},"metadata":null,"id":5973863004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"138","title":"Senior Clinical Trial Associate","company_name":"Definium Therapeutics","first_published":"2026-04-17T16:40:07-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;The Senior Clinical Trial Associate, Clinical Operations, plays a key role in administratively supporting the planning, execution, and management of clinical trials within the organization. The Senior CTA works closely with the clinical operations team to ensure the successful implementation of clinical trials, adherence to regulatory guidelines, and the collection of high-quality data.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Clinical Trial Associate is a senior administrative role and will provide mentorship and guidance to the junior Clinical Trial Assistant role.\u0026amp;nbsp; The Senior Clinical Trial Associate will also support the development and review of Clinical Operations Department Administrative SOPs, Plans and System build.\u0026amp;nbsp; In addition, the Senior CTA will support the design and structure of the Admin framework and implementation of new processes or improvements to current process create processes not currently in place. The Senior Clinical Trial Associate may take ownership and manage sub-projects within the trial (ex: DEA Schedule I oversight at the site and central trial levels) and work closely with key consultants to drive the successful implementation and oversight of sub-projects.\u0026amp;nbsp; They will be the point of contact for all administrative needs for third-party vendors used within a trial and may have some oversight on monthly financial reporting and tracking.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;PRINCIPAL RESPONSIBILITIES:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Establishes, performs quality control, maintains, and archives the Trial Master File (i.e., electronic folder set-up, filing, tracking, archiving) in compliance with DIA Reference Model, SOPs, ICH and GCPs. Ensures prper naming conventions are followed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with study start-up, including development of budgets, contracts, financial disclosure statements, and grant payments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinates distribution of documents and supplies/dosing room materials to sites and vendors/CRO as necessary\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develops and maintains spreadsheets and other documents to track critical study milestones Tracks and reports on project or study information regarding subject and site status, metrics, lab sample shipments and discrepancies, and other parameters as appropriate\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track and manage study-related documentation, including regulatory submissions, ethics committee approvals, and site contracts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepares or assists with the preparation and review of study-related materials as it pertains to CTA processes (e.g., study reference manual, clinical trial material requests, and Investigator Site File)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organizes study information on the shared file drives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain trial Storyboard\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and manage project-based assignments in support of clinical trials (ex: creating process documents and trackers; managing Schedule I activities)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and create process/guidance documents for the Clinical Trial Assistant role-based tasks and responsibilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the writing and review of SOPs for the Clinical Operations department and support systems build out (ex: CTMS, eTMF, etc)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs assigned administrative activities in a timely manner in support of clinical trials from design to completion\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sets up and attends meetings, takes thorough meeting notes, and updates and distributes meeting minutes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organizes and helps plan meetings. May interact with meeting planners and travel agents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinates the distribution of communications to all sites (e.g., questionnaires, newsletters, mass mailings, IND safety reports, Investigator’s Brochures, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists the Clinical Operations Trial Lead with tracking and processing of vendor or site invoices and ensures accurate accrual records are kept for the trials.\u0026amp;nbsp; Raise PO requests and request tax documents from vendors and consultants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains up-to-date knowledge of current regulations and guidelines to ensure compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides general administrative support to the clinical team as assigned\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Processes forms, requests for information by the team, and requests to obtain information from vendors and investigative sites\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide guidance, mentorship, and daily oversight for more junior Clinical Trial Assistants assigned to specific clinical studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for obtaining license agreements for all ClinRo/PROs/scales and updating license holders as required per contract\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;EDUCATION AND EXPERIENCE REQUIREMENTS:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree or equivalent combination of education/experience in science or health-related field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in clinical research, preferably as a Senior Clinical Trial Assistant or with at least 2 years in the Clinical Trial Assistant role\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in Psychiatry and addiction medicine preferred\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness and ability to travel up to 5-10% of the time, defined by business needs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of GCP/ICH guidelines and the clinical development process, understanding of drug development from pre-IND through NDA\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in development of tools and other tracking documents that support clinical research\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with supporting study startup activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills with outside vendors and contractors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willing to maintain flexible work hours as needed and available during core business hours during critical periods of a trial\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong working knowledge of MS Project or Smartsheet\u0026amp;nbsp; and developing Gantt charts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advance knowledge of MS Excel/Google Sheets\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent oral, written, and communication skills required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Problem-solving and strategic planning skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excited by innovative ideas in clinical research space; has a voice and provides meaningful contributions in meetings/calls\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated, resourceful with getting the job done attitude in a fast-paced team environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engaging, empathetic and dynamic personality; up for challenges and determined to find solutions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This position requires strong organizational skills, attention to detail, and the ability to work effectively in a fast-paced and dynamic environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $91,943.00 - $112,330.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4037870004,"name":"35 - Clinical Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5995340004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5154542004,"location":{"name":"Remote"},"metadata":null,"id":5995340004,"updated_at":"2026-06-04T09:56:40-04:00","requisition_id":"148","title":"Senior Cloud Engineer","company_name":"Definium Therapeutics","first_published":"2026-06-04T09:56:40-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Definium\u0026amp;nbsp;Therapeutics is seeking a Senior Cloud Engineer to drive the design, build, and operations of scalable, secure, and automated cloud solutions across the enterprise. This role is highly tactical, focused on day-to-day execution that directly\u0026amp;nbsp;impacts\u0026amp;nbsp;business operations, while ensuring alignment with long-term IT architecture, security, and regulatory requirements.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:240,\u0026amp;quot;335559739\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;The Senior Cloud Engineer will serve as a critical interface between IT engineering, AI/ML teams, software development, data system owners, and business stakeholders, translating business requirements into scalable, compliant, and repeatable technical solutions.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:240,\u0026amp;quot;335559739\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;This role plays a key\u0026amp;nbsp;part\u0026amp;nbsp;in advancing cloud infrastructure, enabling intelligent automation, supporting system integrations, and ensuring operational excellence across\u0026amp;nbsp;Definium’s\u0026amp;nbsp;technology ecosystem.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:240,\u0026amp;quot;335559739\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span data-contrast=\u0026quot;none\u0026quot;\u0026gt;\u0026lt;span data-ccp-parastyle=\u0026quot;heading 2\u0026quot;\u0026gt;Responsibilities\u0026lt;/span\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;134245418\u0026amp;quot;:true,\u0026amp;quot;134245529\u0026amp;quot;:true,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:299,\u0026amp;quot;335559739\u0026amp;quot;:299}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559683\u0026amp;quot;:0,\u0026amp;quot;335559684\u0026amp;quot;:-2,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Design\u0026amp;nbsp;deploy\u0026amp;nbsp;maintain\u0026amp;nbsp;optimize\u0026amp;nbsp;and automate scalable secure and resilient cloud infrastructure and solutions across Azure GCP and AWS\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559683\u0026amp;quot;:0,\u0026amp;quot;335559684\u0026amp;quot;:-2,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Manage backup and disaster recovery strategies across cloud platforms\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559683\u0026amp;quot;:0,\u0026amp;quot;335559684\u0026amp;quot;:-2,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Implement and maintain robust cloud security controls aligned with industry standards CIS NIST and ISO 27001\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559683\u0026amp;quot;:0,\u0026amp;quot;335559684\u0026amp;quot;:-2,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Implement and maintain Infrastructure as Code cloud automation and CI CD driven deployments\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559683\u0026amp;quot;:0,\u0026amp;quot;335559684\u0026amp;quot;:-2,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Support cloud automation initiatives including infrastructure automation integrations operational workflows and platform stability improvements\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559683\u0026amp;quot;:0,\u0026amp;quot;335559684\u0026amp;quot;:-2,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Enable AI and intelligent automation use cases in alignment with established governance and security standards\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559683\u0026amp;quot;:0,\u0026amp;quot;335559684\u0026amp;quot;:-2,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Troubleshoot cloud platform issues support incident resolution and maintain technical documentation and runbooks\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; 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data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559683\u0026amp;quot;:0,\u0026amp;quot;335559684\u0026amp;quot;:-2,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Translate functional and technical requirements into solution architecture and provide build and deployment guidance to software developers\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559683\u0026amp;quot;:0,\u0026amp;quot;335559684\u0026amp;quot;:-2,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Design scalable supportable systems by selecting technology stacks that can be supported by a broad ecosystem of providers and technically skilled Definium staff\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; 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data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559683\u0026amp;quot;:0,\u0026amp;quot;335559684\u0026amp;quot;:-2,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Stay current on leading and emerging technologies and evaluate fit against financial security and operational requirements\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Cross train and mentor junior engineers\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span data-contrast=\u0026quot;none\u0026quot;\u0026gt;\u0026lt;span data-ccp-parastyle=\u0026quot;heading 2\u0026quot;\u0026gt;Qualifications\u0026lt;/span\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;134245418\u0026amp;quot;:true,\u0026amp;quot;134245529\u0026amp;quot;:true,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:299,\u0026amp;quot;335559739\u0026amp;quot;:299}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Bachelor\u0026#39;s degree in Information Systems, Engineering, Business Administration, Computer Science, or related field. MBA or advanced degree preferred\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Minimum 8 years of experience in engineering, infrastructure, or operations roles, preferably in a regulated industry \u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Experience with public cloud platforms (Azure, AWS, or GCP)\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Strong expertise in cloud architecture, networking, and security best practices\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Experience with multi-cloud environments and cloud migrations\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Proficiency in scripting languages such as Python and PowerShell\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Experience implementing enterprise integrations.\u0026amp;nbsp;(APIs, middleware, event-driven systems)\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Experience working within a Microsoft enterprise environment, including:\u0026lt;/span\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Microsoft 365 (M365 / O365\u0026lt;/span\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Entra ID\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Exchange Online\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;SharePoint Online\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Experience with Robotic Process Automation (RPA) and low-code/no-code platforms.\u0026amp;nbsp;(e.g., Microsoft Power Platform)\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:2,\u0026amp;quot;335559739\u0026amp;quot;:0,\u0026amp;quot;335559740\u0026amp;quot;:300}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Familiarity with serverless computing.\u0026amp;nbsp;(Azure Functions, AWS Lambda, Google Cloud Functions)\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:2,\u0026amp;quot;335559739\u0026amp;quot;:0,\u0026amp;quot;335559740\u0026amp;quot;:300}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Experience integrating SaaS applications using middleware platforms\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Cloud architecture certifications such as Azure Solutions Architect (preferred), AWS Certified Solutions Architect, or Google Professional Cloud Architect\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $132,400,00- $170,864.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134233117\u0026amp;quot;:false,\u0026amp;quot;134233118\u0026amp;quot;:false,\u0026amp;quot;335551550\u0026amp;quot;:0,\u0026amp;quot;335551620\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:240,\u0026amp;quot;335559739\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;","departments":[{"id":4037862004,"name":"16 - IT/Facility","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5808053004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5054022004,"location":{"name":"Remote"},"metadata":null,"id":5808053004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"114","title":"Senior Director, Clinical Development","company_name":"Definium Therapeutics","first_published":"2026-02-18T23:16:12-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;The Sr. Director, Clinical Development will play a key role in the design and execution of ongoing and new clinical studies and contribute to the clinical development plan for one or more programs. The position will successfully lead and/or serve as the clinical science representative on one or more clinical studies (US and/or global) to deliver high quality data for registration. The position requires the ability to partner with Clinical Operations, Clinical Pharmacology, Regulatory, Early Development, Medical Affairs, Commercial and other stakeholders to deliver clinical programs for registration and launch. The successful candidate will have direct and recent experience in late phase clinical development, and in CRO and KOL interactions.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provides clinical science leadership within assigned teams or programs\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage the design, planning and execution of clinical trial program(s) as needed with minimal guidance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Is able to play a leadership role in subject matter expertise when interacting with global health authorities\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Has deep familiarity with registration submission strategies and can manage the Clinical needs for all submissions as needed\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Leads the study design, implementation and execution of clinical trials on assigned programs. Is responsible for the preparation of clinical study synopses and serves as a major contributor to the writing of protocols/major amendments, the design of data collection systems, the interpretation of clinical data, and the preparation of final clinical study reports\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Works cooperatively with project team members to provide clinical development expertise and leadership\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Responsible for identifying and cultivating relationships with relevant national and international thought leaders to further project goals\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In partnership with Regulatory Affairs and Project Management, oversee and ensure the quality, coordination and timeliness of clinical sections of IND\u0026#39;s, Investigator Brochures, CTA\u0026#39;s, ISS\u0026#39;, ISE\u0026#39;s and clinical expert reports, including writing and editing  \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Responsible for providing or supervising medical monitoring activities for all human clinical trials including support of adverse event reporting and safety management\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Responsible for ongoing benefit/risk assessment, monitoring adherence to protocols, helping in the investigation of protocol deviations and providing leadership for monitoring activities related to execution of the protocol or program\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provides medical/clinical information for inclusion in reports submitted to regulatory authorities and supports the authoring of regulatory documents\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develops relationships with investigators and external organizations and experts to optimize study design and executions\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Doctoral level degree (PhD, MD, PharmD, PsyD) required \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;6+ years of relevant clinical development experience\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in CNS development (Psychiatry or neurology) strongly preferred\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Possess strong knowledge of the clinical development process\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Possess a solid understanding of the pharmaceutical industry, company competition and commercial side of business\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in small molecule development\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experienced in data review and analysis, presentations (internal and external) and regulatory writing (IND, CTD sections)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience building strong relationships within cross-functional groups to achieve results\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to identify and solve relevant problems related to clinical development\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in clinical research for psychiatry, addiction psychiatry, and addiction medicine programs, strongly preferred.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Background and proven relevant experience in engaging with clinical trial strategy and trial management\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Understanding of the drug development process including technical, business, and regulatory issues.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;IND experience strongly preferred\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Diplomacy and professionalism, ability to build positive relationships both with company leadership and external experts\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Able to command respect from peers and subordinates, capable of highly independent work as well as being a team player and role model\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, verbal and written communication skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to work remotely and with remote internal and external interdisciplinary teams\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Problem-solving and strategic planning skills \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excited by innovative ideas in clinical research space\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated, resourceful with a ‘get the job done’ attitude in a fast-paced team environment\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Other Skills:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excellent writing and communication skills \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Managerial skills a plus\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ability to handle obstacles and roadblocks by anticipating challenges and preparing well thought out arguments and contingencies\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of garnering support for projects and recommendations through on-going collaboration, open and influential communications and commitment to improvement/change\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Special Working Conditions:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Ability to travel as required, including international travel. Average 10-20%, reaching 50% or more in some months\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $247,649.00 - $298,800.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;","departments":[{"id":4037866004,"name":"25 - Clinical Development","child_ids":[4096939004,4103605004],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5985751004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5149124004,"location":{"name":"Remote"},"metadata":null,"id":5985751004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"144","title":"Senior Director, Marketing","company_name":"Definium Therapeutics","first_published":"2026-04-30T14:29:57-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics, formerly known as Mind Medicine, is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Our mission is to be the global leader in the development and delivery of treatments that unlock new opportunities to improve patient outcomes. We are developing a pipeline of innovative product candidates, with and without acute perceptual effects, targeting neurotransmitter pathways that play key roles in brain health.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Founded in 2019, we are continuously expanding our presence and global footprint. We are constantly searching for high-impact individuals in various clinical, technical and business operations domains to strengthen our team of patient-centric, intelligent individuals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director, Marketing leads the development and execution of strategic marketing plans to drive the commercial launch and success of DT120, working closely with regulatory, medical, and sales teams to align with corporate goals. This role involves interpreting complex clinical data, managing brand lifecycles, and ensuring compliance with stringent regulatory standards (e.g., FDA)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop annual marketing plans, brand strategies, and value propositions for DT120\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the entire product lifecycle from pre-launch to post-launch, including market assessment, segmentation, and differentiation, execution, measurement, and optimization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee the promotional review process (MLR/PRC) to ensure all marketing materials, including digital and print, are compliant\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with R\u0026amp;amp;D, Medical Affairs, Market Access, and Sales teams to shape evidentiary needs and support commercial objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct external advertising/media/market research agencies and manage marketing budgets to ensure high-ROI initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive digital strategy, including Veeva systems, social media, and web initiatives to engage Healthcare Professionals (HCPs) and patients\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and build relationships with Key Opinion Leaders (KOLs) to support scientific exchange and brand positioning.\u0026amp;nbsp; Drive congress and advisory board planning and execution\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Life Sciences, Marketing, Business or related discipline, advance degree preferred (MBA preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 15 years in the pharmaceutical, biotech, or healthcare consulting industry, with experience in product launch and brand management\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of pharmaceutical regulations governing HCP and consumer promotion\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with HCP and Patient/Consumer marketing required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to lead, mentor, and build high-performing teams, often in a matrixed environment required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in analyzing market trends, competitive intelligence, and financial models for forecasting\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled with cross functional collaboration and astute at influence, curious to learn from others, driven to share outputs and socialize commercial strategy and objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with REMS product preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Launch experience in the US market required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to synthesize complex data into actionable strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong presentation skills and ability to influence senior, cross functional and sales team stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel as required.\u0026amp;nbsp; Average 10-20%, reaching 50% or more in some months\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $251,775.00 - $294,965.00 Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4069025004,"name":"17 - Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5973783004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5144218004,"location":{"name":"Remote"},"metadata":null,"id":5973783004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"136","title":"Senior Director, Medical Affairs Operations and Strategy","company_name":"Definium Therapeutics","first_published":"2026-04-17T15:54:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In collaboration with Medical Affairs leadership, develop, operationalize, and continuously refine the Medical Affairs strategy, helping to translate strategic objectives into actionable project plans, KPIs and timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and ensure the quality of the departmental strategic planning processes, including operations tasks, and other activities related to pipeline compounds\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leads organization, updating and communication of strategic plans to internal and external stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster strong partnerships with internal teams such as Clinical Development, HEOR, Commercial teams, \u0026amp;amp; finance to ensure alignment and efficiency in medical activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, maintain, and update Medical Affairs SOPs and quality documentation to support compliant, efficient, and consistent operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work in close collaboration with Compliance, Regulatory, and Legal counterparts to deelop materials that that align with regulatory requirement and industry best practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement and refine operational governance frameworks for scientific review and medical communication standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures material development for internal and external use is aligned with organizational goals and priorities and meets compliance, regulatory, and legal requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and oversee project management frameworks for all MA initiatives, including medical launches, clinical collaborations, evidence-generation programs, and scientific communication outputs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor timelines, risks, and deliverables; provide transparent reporting to leadership on progress and resource needs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinates cross-functional project teams to ensure timely execution and integration of medical insights into decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintenance of program budget trackers and financial forecast for Medical Affairs programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement and optimize systems and tools to enhance productivity and data management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and track key performance indicators (KPIs) to measure the effectiveness Medical Affairs operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with IT to implement and optimize technology solutions for medical operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a liaison between Global Medical Affairs and other departments to facilitate smooth operations and communication across regions\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Skills and Competencies:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of Global Medical Affairs functions and their interconnections with other departments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Technical knowledge in Veeva CRM, Veeva Vault, KOL Mapping Systems, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent project management skills with the ability to manage initiatives simultaneously\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to work effectively with cross-functional teams in changing environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Innovative mindset with the ability to identify and implement creative solutions for global challenges\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Doctorate degree (PharmD, MD, DO, PhD)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10 plus years of industry experience with demonstrated high-level professional knowledge and skills in the areas of medical affairs and R\u0026amp;amp;D\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in both pre launch and post-launch medical affairs activites. Experience with Psychiatry/CNS is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to create and lead successful cross-functional teams in changing and competitive environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Early Access Programs (EAP) is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Candidates must be comfortable working independently in a fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $269,204.00 - $295,000.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;","departments":[{"id":4103605004,"name":"27 - Medical Affairs","child_ids":[],"parent_id":4037866004}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5985375004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5148924004,"location":{"name":"San Diego, California"},"metadata":null,"id":5985375004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"143","title":"Senior Manager, Accounting","company_name":"Definium Therapeutics","first_published":"2026-04-30T10:39:08-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Reporting to the Corporate Controller, the \u0026lt;strong\u0026gt;Sr. Manager, Accounting\u0026lt;/strong\u0026gt; will play a key role in our accounting team, with a strong emphasis on SOX 404(b) compliance and equity (stock-based compensation) accounting. This role will be responsible for designing, implementing, and maintaining internal controls, as well as overseeing the accounting and reporting for equity transactions in a fast-paced, public company environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee accounting for stock-based compensation, including stock options, RSUs, PSUs, and ESPP\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure accurate and timely recognition of equity compensation expense in accordance with ASC 718\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage equity-related reports and data from Shareworks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and validate fair value assumptions (e.g., Black-Scholes inputs, peer companies)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with Legal, HR, and external valuation specialists on equity grants and modifications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support preparation of equity disclosures for SEC filings (10-K, 10-Q, proxy)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help lead the design, implementation, and ongoing maintenance of internal controls in compliance with SOX 404(b)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with internal and external auditors to support control walkthroughs, testing, and remediation efforts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate control deficiencies and drive timely remediation plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain and update process flowcharts, risk control matrices (RCMs), and control documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure readiness for external auditor attestation under SOX 404(b)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross-functionally to strengthen control environment and ensure adherence to company policies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support month-end and quarter-end close processes related to equity and other assigned areas\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support commercial-related initiatives that intersect with equity compensation and SOX controls, including evaluation of control impacts from new or evolving processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other accounting, compliance, and internal control-related responsibilities as needed to support the company’s financial reporting and growth objectives\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required, degree in Accounting, Finance, or related field preferred, CPA License preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 7 years of progressive accounting experience required, life science industry preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience with Shareworks and NetSuite preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience with equity administration and technical accounting required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience with accounting in a publicly traded company required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting accounting or SOX considerations related to commercial operations, business process changes, or company scale-up initiatives preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep, hands-on knowledge of SOX 404(b) requirements and internal control frameworks (e.g., COSO)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills, along with the ability to present numeric data effectively\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience working with external auditors in a SOX-compliant environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to handle highly confidential information with sound judgment and discretion\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Intermediate-to-advanced MS Office skills (Outlook, Word, Excel, PowerPoint)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Please note that you must come into the San Diego, CA office once a week\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $145,940.00 - $171,503.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;","departments":[{"id":4052052004,"name":"12 - Finance","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/6001473004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5157111004,"location":{"name":"Remote"},"metadata":null,"id":6001473004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"151","title":"Senior Product Manager, HCP Marketing","company_name":"Definium Therapeutics","first_published":"2026-05-20T17:35:37-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is seeking a highly motivated \u0026lt;strong\u0026gt;Senior Product Manager, HCP Marketing\u0026lt;/strong\u0026gt; to support the development and execution of HCP marketing strategy for our lead brand.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the Senior Director, Marketing this individual will play a key role in shaping and implementing HCP promotional initiatives to support launch readiness and commercial success. The role requires a strategic, hands-on marketer who can translate brand strategy into impactful execution across personal and non-personal promotion, while effectively leading day-to-day collaboration with Definium’s Agency of Record (AOR) and cross-functional internal stakeholders.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate brings strong pharmaceutical marketing experience, proven HCP promotional expertise, and the ability to thrive in a fast-paced, entrepreneurial biotech environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support development and execution of HCP marketing strategy aligned with brand objectives and commercial priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to brand planning, launch readiness, and tactical planning processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help shape HCP promotional strategy and messaging based on customer insights, market dynamics, and competitive intelligence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate complex scientific and clinical data into clear, compelling HCP-focused promotional narratives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify opportunities to optimize HCP engagement across customer touchpoints and channels\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead development and execution of HCP promotional initiatives to support brand performance and launch objectives establishing scalable commercial processes and operating discipline within a growing organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own assigned promotional workstreams from strategy through execution, measurement, and optimization ensuring flawless delivery while balancing speed, quality and compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop tactical plans aligned with approved strategic direction, including timelines, budgets, and execution plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as primary day-to-day marketing lead with the AOR across HCP promotional initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide clear strategic direction, feedback, and decision-making to agency partners to ensure high-quality deliverables \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with Medical, Regulatory, Legal, Commercial Operations, Sales, Market Access, Analytics, and Market Research teams to drive aligned execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead promotional materials through review and approval processes in partnership with cross-functional stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leverage market research, analytics, field insights, and competitive intelligence to inform decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor performance of promotional initiatives and identify opportunities for optimization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage HCP marketing budgets across assigned initiatives tracking timelines, milestones, deliverables, and agency spend\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum bachelor’s degree required; advanced degree (MBA, PharmD, MS, or related field) preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 7 years pharmaceutical or biotech commercial experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;HCP marketing experience with demonstrated promotional ownership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience developing and executing HCP promotional campaigns\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to translate scientific complexity into effective commercial promotion\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong strategic thinking with demonstrated executional excellence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong cross-functional collaboration and stakeholder management capabilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication and platform skills (will be the face of marketing to the field force)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analytical mindset with ability to draw actionable insights from multiple data sources\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing agency partners required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working within promotional review / MLR processes required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Launch experience strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;CNS / psychiatry / specialty pharmaceutical experience preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in small biotech or fast-paced growth environments strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Up to 40% travel will be required based upon business needs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $170,000.00 - $197,911.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4037872004,"name":"11 - Marketing","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5836395004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5068234004,"location":{"name":"Remote"},"metadata":null,"id":5836395004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"118","title":"Senior Project Manager","company_name":"Definium Therapeutics","first_published":"2026-03-24T16:55:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate enjoys working in a rapidly growing environment with strong focus on execution, navigating multiple stakeholders and priorities, and has an excellent understanding of formal project management methodologies, preferably including experience in using Planisware Enterprise.\u0026amp;nbsp; The Sr. Project Manager will lead the development of Project plan(s) to support functional areas or workstreams. Closely and proactively monitor the execution of the project plans and deliverables to ensure successful delivery of the program milestones, company milestones, and objectives. Anticipate potential risks and problems (e.g. resource bottlenecks, risks to critical milestones, inefficient processes) and proactively develop risk mitigation plan.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and interpersonal skills. Networking and stakeholder management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in a highly matrixed organization with geographically dispersed teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Problem solving and decision-making skills. Demonstrated ability to drive initiatives, solve issues (conflict management and facilitation skills), anticipate problems and achieve objectives, while keeping an eye on the big picture\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic and analytical thinking skills to assimilate complex information, operate effectively in situations of ambiguity and simplify complex issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding/experience working within a functional area such as clinical, preclinical, CMC or regulatory affairs would be considered beneficial\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Full understanding of drug development business processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High competence in use of Microsoft Office, Microsoft Project or equivalent and other PM appropriate tools\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Planisware Enterprise and Office Timeline is preferred but not required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s Degree with 8+ years’ experience in the Pharmaceutical / Biotech industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 5+ years\u0026#39; experience in project/program management roles in the pharma/biotech industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in late phase development organizations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with NDA submissions is preferable\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity of working with clinical trials from a project/program management stance\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $130,000.00 - $160,403.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4076011004,"name":"30 - Program Management","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5991707004","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":5152191004,"location":{"name":"Remote"},"metadata":null,"id":5991707004,"updated_at":"2026-06-01T15:27:03-04:00","requisition_id":"146","title":"Vice President, Sales","company_name":"Definium Therapeutics","first_published":"2026-05-08T14:39:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our lead\u0026amp;nbsp;product\u0026amp;nbsp;candidate,\u0026amp;nbsp;lysergide\u0026amp;nbsp;tartrate\u0026amp;nbsp;(our\u0026amp;nbsp;proprietary orally disintegrating tablet form of\u0026amp;nbsp;lysergide\u0026amp;nbsp;(LSD) D-tartrate),\u0026amp;nbsp;represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Guided by\u0026amp;nbsp;the recognition\u0026amp;nbsp;that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address\u0026amp;nbsp;the\u0026amp;nbsp;underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Together we are moving psychiatry forward—beyond better, into a boundless future. Join us!\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;We are seeking an experienced and visionary Vice President of Sales to lead the sales field team and sales training efforts in preparation for the potential commercial launch of DT120. This senior leadership role will focus on building and scaling a high-performing sales organization while driving successful product launches in the psychiatry space.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the Chief Commercial Officer, the ideal candidate will have proven expertise launching products in the neuroscience or CNS therapeutic area (ideally with experience in complex and/or REMS products), a strong track record of building high-caliber sales teams as a Vice President, and the ability to foster a collaborative, positive sales culture grounded in the highest integrity. This role involves cross-functional coordination with other field teams (i.e. reimbursement specialists, site readiness team, and others).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a high-impact, hands-on leadership position for a strategic sales leader passionate about advancing transformative treatments for brain health.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Key Responsibilities\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and Lead the Sales Field Team: Recruit, develop, mentor, and retain a high-caliber national sales team. Provide ongoing coaching, performance management, and leadership to ensure the team meets or exceeds sales targets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee Sales Training: Design, implement, and continuously improve comprehensive sales training programs to equip the field team with deep product knowledge, selling skills, and expertise in the neuroscience/CNS landscape\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive Product Launch: Lead the execution of sales strategies and tactical plans for DT120, contributing to rapid market adoption and revenue growth\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cross-Functional Coordination: Partner closely with the commercial operations team and other functions to ensure territory mapping, deployment scenarios, and resource allocation are adequate and optimized. Facilitate effective collaboration across commercial teams (e.g., with marketing, medical affairs, and market access) to support integrated pull-through initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;REMS and Specialty Expertise: Apply experience with Risk Evaluation and Mitigation Strategy (REMS) programs or other complex distribution models to guide compliant and effective sales execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster Sales Culture: Cultivate a collaborative, inclusive, and high-integrity sales culture that emphasizes ethical practices, accountability, teamwork, and a patient-centric mindset\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performance Management \u0026amp;amp; Insights: Establish clear KPIs, monitor field performance, and provide regular feedback and adjustments. Share field insights with cross-functional partners to refine commercial strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Compliance: Ensure all sales activities adhere to the highest ethical standards, regulatory requirements, and company policies\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Qualifications:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; advanced degree (MBA, PharmD, or related) strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 15 years of progressive pharmaceutical/biotech sales leadership experience, with at least 3 years in a Vice President of Sales (or equivalent senior sales leadership) role\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of successfully building and leading sales field teams from planning through launch and growth\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience launching products in the neuroscience, CNS, or psychiatry therapeutic area\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with REMS programs or other highly regulated/complex commercialization models\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success in cross-functional coordination with commercial operations, reimbursement, market access, or site-of-care teams (without direct line management of those functions)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leadership \u0026amp;amp; Personal Attributes:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Exceptional ability to build, inspire, and develop high-performing sales teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highest level of personal and professional integrity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong collaborator who excels at cross-functional partnerships\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinker with excellent communication, influencing, and analytical skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Passion for mental health innovation and patient-centered sales execution\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to travel extensively (up to 50–70%) to support the field team, training initiatives, and key stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;What We Offer\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive compensation package, including base salary, performance bonus, equity, and comprehensive benefits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Opportunity to play a pivotal role in building the sales foundation for groundbreaking therapies that could transform psychiatry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative, mission-driven culture at a company with a high-profile late-stage pipeline and significant 2026 catalysts.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;The starting base pay range for this position is $322,103.00 - $380,000.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;100% paid health benefits including Medical, Dental and Vision for you and your dependents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with company match and vesting after the turn of the first month after your start date\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generous parental leave and some fun fringe perks!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;","departments":[{"id":4069025004,"name":"17 - Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4023844004,"name":"Remote US","location":null,"child_ids":[],"parent_id":null}]}],"meta":{"total":20}}