{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5228687008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4478869008,"location":{"name":"Burlington, MA"},"metadata":null,"id":5228687008,"updated_at":"2026-05-21T20:59:33-04:00","requisition_id":"COMM-26-01","title":"Associate Director, Commercial Strategy and Insights","company_name":"MapLight Therapeutics","first_published":"2026-05-21T20:59:33-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly motivated Associate Director, Commercial Strategy and Insights to support the development and execution of commercial initiatives across our growing organization. This role will help build market research, forecasting, and competitive intelligence that inform launch planning, market opportunity assessments, and commercial strategy for our lead asset and broader pipeline. As the commercial function grows, the role is expected to evolve into a role on our Insights and Analytics team.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director will work closely with Commercial Leadership, Marketing, Market Access, Medical Affairs, Sales, Finance, Business Development, and Clinical teams to inform data-driven strategies that maximize product value and support long-term company growth. The ideal candidate combines analytical rigor, strategic thinking, and strong cross-functional collaboration within a fast-paced pre-commercial biotech environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support market research, forecasting and analytics workstreams that inform integrated commercial strategies for our lead asset and pipeline products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct market assessments, competitive analyses, and opportunity evaluations to inform strategic decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with cross-functional teams to define product positioning, target customer segments, and value propositions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support commercial launch planning activities for new products and indications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify commercial risks, opportunities, and mitigation strategies throughout launch planning and execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in development of launch KPIs, performance metrics, and tracking dashboards.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Monitor the market landscape, including lead and emerging competitors, payer trends, and congress data. Synthesize findings for senior leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Synthesize primary and secondary market research into actionable insights for commercial planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development of executive presentations, strategic recommendations, and board materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze syndicated prescription, claims, and formulary data to identify trends that inform commercial planning\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Help drive alignment between corporate objectives and commercial execution plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain commercial forecasts, including patient-based and epidemiology-based models, and update assumptions as new data emerge.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain reporting tools and dashboards to monitor key business metrics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Utilize data analytics to inform strategic recommendations and resource allocation decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide commercial input into Phase 3 design, target product profile, and label discussions in collaboration with Corporate Strategy, Regulatory, Clinical Development and Medical Affairs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operate within pre-approval compliance requirements governing promotional activity, payer communications, and HCP interactions.\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 Business, Life Sciences, Economics, Marketing, or related field required; MBA or advanced degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years of experience in biotechnology, pharmaceuticals, healthcare consulting, commercial strategy, or related function.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in commercial planning, market research, forecasting, or analytics within biotech or specialty pharmaceutical environments. Pre-launch or first commercial launch experience preferred. CNS, psychiatry, or specialty neuroscience therapeutic exposure preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong strategic thinking and analytical problem-solving abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and presentation skills with ability to influence stakeholders at multiple levels.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience conducting market analysis, forecasting, and competitive intelligence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced proficiency in Excel and PowerPoint; familiarity with commercial analytics and visualization tools preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple priorities in a dynamic, fast-paced pre-commercial environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong collaboration and cross-functional leadership capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Background in launch excellence, market access strategy, or commercial operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with syndicated pharmaceutical datasets and conducting market research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with CRM platforms, forecasting tools, and business intelligence systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of pre-approval promotional and compliance regulations.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a hybrid role on-site 3 days per week in our offices in Redwood City, CA or Burlington, MA.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Ability to travel as needed (up to 20%) for corporate and department-wide meetings.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$195,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$220,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017887008,"name":"Commercial","child_ids":[],"parent_id":4064591008}],"offices":[{"id":4012956008,"name":"Burlington","location":"Burlington, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5209830008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4469557008,"location":{"name":"Remote"},"metadata":null,"id":5209830008,"updated_at":"2026-06-04T18:37:19-04:00","requisition_id":"DD-26-02","title":"Associate Director, Medicinal Chemistry","company_name":"MapLight Therapeutics","first_published":"2026-05-04T18:30:36-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do: \u0026lt;/strong\u0026gt;We are searching for a highly motivated Medicinal Chemist to join our drug discovery team at the Associate Director level.\u0026amp;nbsp; Reporting to the Executive Director of Chemistry, the candidate will be expected to co-lead, or lead, preclinical medicinal chemistry programs from hit to candidate nomination. A highly qualified candidate will have experience in CNS drug discovery and an in-depth understanding of designing efficacious and safe brain-penetrant small molecules. While MapLight has in-house laboratories for pre-clinical research, many activities like chemical synthesis are outsourced to external vendors. Experience managing remote CRO teams, logistics across multiple partners, and coordinating internal drug discovery activities across different time zones is essential. This is a fantastic opportunity to join a small medicinal chemistry team and have a significant impact in addressing unmet patient needs by advancing MapLight’s pipeline.\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;Co-lead, or lead, preclinical medicinal chemistry programs from hit to candidate nomination.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and execute successful medicinal chemistry strategies to meet project and corporate goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct multi-parameter optimization to deliver orally bioavailable, brain-penetrant candidates without secondary pharmacology, ADME, or safety concerns of initial hits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply structure-based drug design principles utilizing in-house resources and external computational partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage chemistry and tiered screening cascade at external contract research organizations (CROs).\u0026amp;nbsp; This includes maintaining a good relationship, overseeing synthesis or experimental plans, project tracking, evaluation of results, and assisting in troubleshooting. May require assessment of analytical data including NMR, LCMS, HPLC, UV-VIS, and DSC.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply previous experience with successful hit finding strategies to find novel chemical equity, including scaffold-hopping approaches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with in-house drug discovery team to ensure compounds are distributed in support of other disciplines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide regular project updates to Leadership and Project Teams that include relevant updates. May include in-depth SAR, ADME, and PK analyses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Co-lead, or lead, patent strategy to protect existing or novel chemical matter with Maplight legal partners, when appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You can participate and work effectively with multiple cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You have strong interpersonal skills and understand relationships are key to being successful.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You are a leader. Teams love working with you, and you are someone who takes pride in mentoring and supporting the careers of others.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You’re a team player who is willing to roll-up your sleeves and get the job done.\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;PhD in Chemistry or Medicinal Chemistry with 10+ years’, or BS/MS 15+ years’, pharmaceutical experience successfully (co)leading preclinical drug discovery programs.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contemporary knowledge of Medicinal Chemistry concepts with strong working knowledge of computational chemistry, biology, pharmacology, drug metabolism, and pharmacokinetics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in CNS drug discovery\u0026amp;nbsp;is essential, including a successful track record of delivering brain-penetrant candidate compounds for brain disorders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track record of successfully managing projects remotely through multiple and CRO partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clear record of accomplishments as exemplified through patents and/or publications.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel: \u0026lt;/strong\u0026gt;Candidate can expect to travel 4-6 times a year to meet with collaborators and/or attend both discovery and all-company meetings.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$180,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$205,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017883008,"name":"Drug Discovery","child_ids":[],"parent_id":4064589008}],"offices":[{"id":4012958008,"name":"Remote","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5217402008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4473508008,"location":{"name":"Burlington, MA"},"metadata":null,"id":5217402008,"updated_at":"2026-05-12T11:04:30-04:00","requisition_id":"BIOM--26-03","title":"Associate Director, Statistical Programming","company_name":"MapLight Therapeutics","first_published":"2026-05-12T11:03:59-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Reporting to the Senior Director, Statistical Programming, the Associate Director will provide statistical and clinical data programming expertise to manage statistical programming activities that support drug development programs and regulatory submissions. This role involves overseeing the creation, validation, and delivery of programming deliverables, ensuring compliance with industry standards, and fostering cross-functional collaboration with biostatistics, data management, clinical, and regulatory teams.  \u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee the development and validation of SAS programs to generate datasets (SDTM, ADaM), tables, listings, and figures (TLFs) in compliance with CDISC standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure the timely and high-quality delivery of programming outputs for regulatory submissions, clinical study reports, and exploratory analyses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all programming activities align with industry standards (CDISC, ICH, FDA, EMA) and internal SOPs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Programming lead for clinical programs as needed. Hand-on programming work in SAS and other programming languages/tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establishes and maintains CRO/vendor partnerships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a liaison between statistical programming and other functions, ensuring clear communication and alignment of goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with biostatistics, data management, and clinical operations to resolve programming issues and optimize processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and implement new tools, techniques, and processes to improve efficiency and quality in statistical programming.\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;Master’s degree in statistics, computer science or a related field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 8 years of statistical programming experience in the pharmaceutical/biotech industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to manage CRO relationships and oversee programmed deliverables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience in leading statistical programming function for both early and late phase clinical trials, and regulatory submissions (NDA/BLA, MAA)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent skills in SAS programming and statistical reporting, knowledge of R and R Shiny desirable\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with FDA and ICH regulations and guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills, ability to collaborate with a multidisciplinary team and interact effectively in a fast-paced team environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;This is a hybrid role with three days per week in-office in Burlington, Massachusetts.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$195,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$225,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017897008,"name":"Biometrics","child_ids":[],"parent_id":4064588008}],"offices":[{"id":4012956008,"name":"Burlington","location":"Burlington, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5215770008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4472646008,"location":{"name":"Burlington, MA"},"metadata":null,"id":5215770008,"updated_at":"2026-05-12T01:00:58-04:00","requisition_id":"BIOM-26-02","title":"Clinical Data Manager","company_name":"MapLight Therapeutics","first_published":"2026-05-11T10:18:29-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly skilled and motivated Clinical Data Manager to join our Clinical Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role in ensuring the integrity, accuracy, and completeness of clinical trial data, contributing to the successful development and regulatory approval of our products.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage and lead all aspects of clinical trial data management activities from study start-up to database lock.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement data management plans, data validation plans, edit check plans and data entry guidelines in compliance with regulatory standards and company SOPs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross-functional teams including Clinical Operations, Biostatistics, and Regulatory Affairs to ensure data quality and integrity throughout the trial lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee Medidata Rave electronic data capture (EDC) system setup, configuration, user management, coding and data extracts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform data cleaning, discrepancy management, SAE and vendor integration reconciliation activities to ensure timely database lock.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct periodic data reviews and generate weekly data quality metrics to identify trends and outliers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify Protocol Deviations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Produce medical monitor, coding listings and ad hoc listings for team review (Jreview, SAS, Business Objects).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in the development and review of clinical study protocols, case report forms (CRFs), and clinical trial documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide support for regulatory submissions, audits, and inspections related to clinical trial data management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stay current with industry standards, best practices, and regulatory requirements related to clinical data management.\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, computer science, or a related field. Advanced degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5 years of experience in clinical data management within the pharmaceutical or biotechnology industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Medidata Rave electronic data capture (EDC) system..\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of Good Clinical Practice (GCP) guidelines, regulatory requirements (e.g., FDA, EMA), and industry standards (e.g., CDISC).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, organizational, and problem-solving skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work effectively in a fast-paced, cross-functional team environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and commitment to data quality and integrity.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; This is a hybrid position with three days per week onsite at our office in Burlington, MA or Redwood City, CA.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;MapLight does not accept unsolicited resumes from recruiters, staffing agencies, or search firms.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$145,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$160,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017897008,"name":"Biometrics","child_ids":[],"parent_id":4064588008}],"offices":[{"id":4012956008,"name":"Burlington","location":"Burlington, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5211717008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4470504008,"location":{"name":"Burlington, MA"},"metadata":null,"id":5211717008,"updated_at":"2026-05-12T01:00:58-04:00","requisition_id":"LEGL-26-01","title":"Contracts and Legal Systems Manager","company_name":"MapLight Therapeutics","first_published":"2026-05-06T12:42:14-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;An exciting new opportunity has opened up for a Contracts and Legal Systems Manager to assist with our day-to-day legal systems and contracting needs, including for clinical trials, supply, commercial, finance, and other key contracting areas.\u0026amp;nbsp; Reporting to the Company’s Sr. Director, Corporate Counsel, this individual will play a key role in a growing legal team, with many opportunities to grow their career with the company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate should have significant experience working with contracts management systems, including acting as the key legal point of contact for business users, training clients, and managing contracts workflows within a cross-functional team. The ideal candidate should also have significant experience drafting, negotiating, and managing agreements for clinical and commercial-stage pharmaceutical and life sciences companies, including non-disclosure agreements, master services agreements, consulting agreements, manufacturing and supply agreements, clinical trial agreements, and other commercial agreements.\u0026amp;nbsp; Experience as a corporate paralegal or legal support analyst at life sciences companies or law firms is considered a plus.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The successful candidate must be able to take ownership of the legal function’s role in a company’s legal, procurement, and financial systems architecture, as well as work independently to draft, revise and negotiate agreements, with a flexible and collaborative approach.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Be responsible for the operation and administration of the company’s contract management system, acting as the key point of contact for the business\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate and assist in developing policies, procedures and systems to support and facilitate efficient contract development and analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Draft, review and negotiate a variety of day-to-day contracts, including non-disclosure agreements, master service agreements, consulting agreements, manufacturing and supply agreements, clinical trial agreements and other clinical documents, independently and with limited supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Negotiate to conclude agreements as efficiently as possible while meeting client needs and safeguarding MapLight’s interests\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effectively manage outside vendors, including working with and supervising outside counsel, as required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create, improve, and implement applicable forms, templates, processes, and procedures to improve efficiency\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain and maintain a strong working knowledge of the Company’s business, scientific capabilities, and key strategic business objectives\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Other Skills and Abilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Solid business judgment and strategic thinking. Ability to recognize risk and develop practical, workable strategies to mitigate such risk\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexibility and willingness to work on a broad variety of matters\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and oral communications skills required to work both internally and externally.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to independently work with minimal day-to-day oversight\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to meet deadlines while managing a substantial workload in a fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to engender confidence when advising clients at all levels\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work with the highest level of integrity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to travel when required\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 with a minimum of 5 years of progressive responsibility with recent experience in contract negotiation, administration and/or management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with pharmaceutical and life sciences companies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with design and administration of contracts management systems (e.g., Ariba, Coupa, Concur, NetSuite)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paralegal certification or equivalent legal education or training is considered a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive computer skills including Microsoft Office\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key MapLight Behaviors:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We consider these behaviors we seek in all MapLight employees.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;You can participate and work effectively with multiple cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You have strong interpersonal skills and understand relationships are key to being successful.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You are a leader. Teams love working with you, and you are someone who takes pride in mentoring and supporting the careers of others.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You’re a team player who is willing to roll-up your sleeves and get the job done.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Candidates for this role must be within commuting distance of MapLight’s Burlington, MA office.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel:\u0026lt;/strong\u0026gt; Minimal travel (1-2 times per year) is expected.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$130,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$155,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017889008,"name":"Legal","child_ids":[],"parent_id":4064591008}],"offices":[{"id":4012956008,"name":"Burlington","location":"Burlington, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5217336008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4473475008,"location":{"name":"Burlington, MA"},"metadata":null,"id":5217336008,"updated_at":"2026-05-12T10:36:56-04:00","requisition_id":"BIOM-26-04","title":"Director, Biostatistics","company_name":"MapLight Therapeutics","first_published":"2026-05-12T10:36:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;MapLight is looking for an experienced and resourceful Director, Biostatistics.\u0026amp;nbsp; Reporting to Senior Director, Biostatistics, this role will be responsible for the statistical aspects of assigned clinical projects. This is a hands-on role where you will work with internal and external cross-functional study teams, support interaction with Health Authorities, and manage CRO for statistical related deliverables.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide/validate sample size/power calculation and author statistical section of the protocol.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for the development of study SAP and table/figure/listing shells including overseeing CRO’s work.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work collaboratively with Clinical Development, Clinical Operations, Clinical Data Managers, Regulatory and other functions to meet project deliverables and timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide statistical and strategic inputs in documents prepared for regulatory interactions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide technical oversight of statistical activities of external vendors to ensure timeliness and quality of analysis data and statistical outputs. Review and approve key statistical vendor deliverables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to clinical study reports, including authoring of statistical methods and interpretation of the study results.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and contribute to the preparation of publications, including manuscripts, posters and oral presentations.\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;PhD in biostatistics or related discipline with 7+ years, or Master\u0026#39;s Degree with 10+ years of experience in the pharmaceutical or biotech industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability and experience in the design, analysis and reporting of clinical trials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of design considerations. Familiarity with CNS endpoints and associated analysis methodologies highly desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive knowledge of FDA, EMA and ICH regulations and industry standards applicable to the design and analysis of clinical trials and regulatory submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in statistical programming (SAS and R). Experience with trial design software (e.g., EAST).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to concurrently lead statistical efforts for multiple projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding data standards, including SDTM and ADaM.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adept at overseeing statistical services provided by CRO\u0026#39;s.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills; Ability to communicate statistical information to non-scientists, willingness to educate internal team.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;This is a hybrid position with three days per week onsite at our office in Burlington, MA.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$195,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$245,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017897008,"name":"Biometrics","child_ids":[],"parent_id":4064588008}],"offices":[{"id":4012956008,"name":"Burlington","location":"Burlington, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5206405008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4467878008,"location":{"name":"Remote"},"metadata":null,"id":5206405008,"updated_at":"2026-05-12T01:00:57-04:00","requisition_id":"PV-26-01","title":"Director, Safety Scientist, Pharmacovigilance","company_name":"MapLight Therapeutics","first_published":"2026-05-04T10:07:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Safety Scientist will be responsible for high quality safety surveillance activities including medical review of individual case safety reports (ICSRs), aggregate report production, safety governance meeting coordination, safety signal detection and assessment, and safety risk management activities for assigned products. This individual will collaborate with Program Safety Lead and other program team members, pharmacovigilance operations, and CROs to ensure proactive safety surveillance in compliance with global regulations.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\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 safety surveillance and signal detection activities (period review of aggregate safety data, safety surveillance team meetings, track signals and related documentation)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent PV at clinical study team for assigned product\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop signal assessment report under the oversight of Program safety lead for validated safety signal\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with PV operations for timely and accurate medical review of ICSRs for assigned clinical study as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and contribute safety risk management plan across product lifecycle\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and manage periodic reports (DSUR/PBRER)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute for data analysis and authoring of safety sections for regulatory submissions and regulatory responses\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute for the development or updates of safety surveillance and risk management SOPs, templates etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with clinical study teams on safety surveillance deliverables (IB, RSI, Protocol, Briefing documents etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participating in PV audit and inspections\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Pharmacovigilance function in committees and activities both internally and externally when appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We consider these behaviors we seek in all MapLight employees.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;You can participate and work effectively with multiple cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You have strong interpersonal skills and understanding relationships are key to being successful.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You are a leader. Teams love working with you, and you are someone who takes pride in mentoring and supporting the careers of others.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You’re a team player who is willing to roll up your sleeves and get the job done.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Health care professional degree (e.g. RN, BSN, PharmD) or advanced degree (Masters/PhD) in biomedical sciences, pharmaceutical sciences, or related life science.\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Preferred: Post-graduate training in epidemiology (e.g. MPH)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 10 years of pharmacovigilance experience within the biopharmaceutical industry with at least 3 years of direct clinical/patient care experience\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Preferred: Safety surveillance and risk management experience in neuroscience, psychiatry or neurodegenerative disease area\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competence in conducting safety data reviews, preparation of aggregate reports, signal detection and risk management plans for investigational and/or post-marketed products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with MedDRA and drug coding reviews\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated expertise in global PV regulations, GVP and ICH guidelines, safety systems, and drug development processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in PV processes for individual case handling, signal management, aggregate data review, aggregate reports, and audits/inspections\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional communication and cross-functional collaboration skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinker with the ability to translate complex safety data into actionable insights for regulatory and clinical decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to work within a growing organization and to help the organization evolve over time\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to engage in an open, constructive and continuous dialogue with the Company’s stakeholders based on equality and mutual respect\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly motivated, self-driven and dependable\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Committed to MapLight\u0026#39;s Core Beliefs and Values\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp; This is a remote US position.\u0026amp;nbsp; Hybrid 3 day in office policy for anyone located within 50 miles of Redwood City, CA or Burlington, MA.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel:\u0026lt;/strong\u0026gt; Ability to travel as needed (up to 10%) for corporate and departmental meetings.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: \u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt;MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$220,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$240,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017898008,"name":"Pharmacovigilance","child_ids":[],"parent_id":4064588008}],"offices":[{"id":4012956008,"name":"Burlington","location":"Burlington, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5230710008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4479850008,"location":{"name":"Remote"},"metadata":null,"id":5230710008,"updated_at":"2026-06-08T09:33:16-04:00","requisition_id":"CDEV-26-03","title":"Executive Director, Clinical Program Management ","company_name":"MapLight Therapeutics","first_published":"2026-05-26T10:20:09-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Executive Director, Clinical Program Management provides leadership and direction across the MapLight clinical development portfolio, supporting programs across all stages of development. The role is accountable for oversight, functional leadership, and consistency of program management practices, strengthening the quality and effectiveness of program management across Clinical Development. This role reports to the Senior Vice President, Clinical Development and may have one or more direct reports.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\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;Lead the Clinical Program Management function by defining standards, best practices, and continuous improvement initiatives, and by developing the team through coaching, feedback, and role modeling to strengthen Program Management as a discipline within the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be accountable for Clinical Program Management effectiveness across the clinical development portfolio.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Align with leadership to deliver corporate and departmental goals and initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical Leads and cross-functional teams on program planning, deliverables, and timelines, supporting effective execution across the portfolio.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with Nonclinical Program Management on seamless progression of programs from preclinical into clinical development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure quality, consistency, accountability, and responsiveness of the Clinical Program Management function across planning, execution, communication, and governance-related processes as they evolve.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enable high-quality development decision making by anticipating and addressing gaps, misalignment, or inefficiencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Anticipate cross-program risks, conflicts, and resource constraints, and intervene proactively to mitigate issues appropriately.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;We seek these behaviors in all MapLight employees.\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;You can participate and work effectively with multiple cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You have strong interpersonal skills and understand relationships are key to being successful.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You are a leader. Teams love working with you, and you are someone who takes pride in mentoring and supporting the careers of others.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You’re a team player who is willing to roll-up your sleeves and get the job done.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience in biotech or pharmaceutical clinical development, with a documented track record of leadership across complex, multi-stage clinical programs and portfolios.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success operating at both program and portfolio levels, including participation in governance, prioritization, and development decision-making forums.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong grounding in clinical development principles, regulatory strategy, and cross-functional execution sufficient to engage credibly with Clinical Program Leads, functional experts, and senior leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience partnering effectively with Clinical, Regulatory, Operations, CMC, and related functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to apply sound judgment under ambiguity, anticipate risk, and enable high-quality development decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead and develop Program Management professionals while remaining engaged as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced proficiency in enterprise program and portfolio management tools (eg Smartsheet or equivalent), with demonstrated application to enable standardized planning, tracking, and reporting across complex clinical programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective oral and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fluent in written and verbal business English.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly motivated, self-driven and dependable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Committed to MapLight\u0026#39;s Core Beliefs and Values.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Travel:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel, as necessary.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Remote US position.\u0026amp;nbsp; Hybrid 3 days in office for employees located within 50 miles of Redwood City, CA or Burlington, MA.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;MapLight does not accept unsolicited resumes from recruiters, staffing agencies, or search firms.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$276,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$321,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017885008,"name":"Clinical Development","child_ids":[],"parent_id":4064588008}],"offices":[{"id":4012956008,"name":"Burlington","location":"Burlington, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5211630008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4470459008,"location":{"name":"Remote"},"metadata":null,"id":5211630008,"updated_at":"2026-05-12T01:00:57-04:00","requisition_id":"COPS-26-05","title":"Lead CRA","company_name":"MapLight Therapeutics","first_published":"2026-05-06T11:49:22-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the VP of Clinical Operations the Lead Clinical Research Associate will oversee an assigned MapLight study monitoring team to ensure monitoring quality and excellence in line with MapLight’s Mission, Vision, and Values. This role will maintain site management and monitoring responsibilities for assigned sites in addition to study team level work. This role will collaborate closely with key cross-functional internal stakeholders, Clinical Operations, Clinical Development, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendor partners to ensure quality of monitoring conduct and oversight from study start up through close out. This is a highly collaborative and dynamic role within a fast paced and results-oriented environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and manage a team of Clinical Research Associates.\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide line management for CRAs inclusive of performance management and career development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure CRAs are trained and maintain compliance with internal procedures and processes and regulatory requirements (GCP).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the Clinical Operations study team with CRA resourcing.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain site management and monitoring responsibility for at least one site for the assigned study(ies).\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prepare for and conduct Pre-Study, Initiation, Interim and Closeout monitoring visits in accordance with MapLight SOPs and procedures, regulatory requirements and industry guidelines and best practices (ICH GCP).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the study team in meeting study milestones (site activation, DSMB meetings, database lock, etc.).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform centralized monitoring activities between on-site visits to ensure timely resolution of action items, oversight of study data quality and flow, and proactively identify and mitigate/manage study risks and issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain quality and compliant documentation related to all aspects of site management including quality and ALCOA+ compliant monitoring visit reports, centralized monitoring reports, site contact reports, Trial Master File/Investigator Site File, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the main MapLight point of contact for Investigator sites to support protocol compliance, streamlined communications, timely responses to site staff needs, and training needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the study team and Investigator sites during inspections or audits, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the study team(s) in development of study-specific monitoring procedures.\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain the study monitoring plan, templates, and tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recommend and implement appropriate monitoring strategy based on study design, recruitment goals and the needs of the study.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain current knowledge of regulatory requirements and industry best practices related to monitoring, including centralized monitoring and risk-based monitoring.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a core member of the cross-functional study team.\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Participate in study team meetings as a subject matter expert on monitoring processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Take a proactive and innovative approach to risk and issues management as related to monitoring quality or strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recommend and implement process changes related to monitoring to support study goals and timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the study team in the integration of the monitoring function in study management (feasibility, site activation, site communication, risk management, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the study team and Investigator sites during inspections or audits, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accomplish other tasks as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide oversight of study monitoring\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Review monitoring visit reports to ensure MapLight quality standards are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review Key Performance Indicators for assigned CRAs to ensure high performance and compliance with requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform oversight visits and co-monitoring visits to ensure quality monitoring.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development and process improvement for the MapLight monitoring function.\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support development and revision of SOPs, processes, templates, tools, and plans with the aim of continual improvement and streamlining.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a forward-thinking approach to monitoring process to support department and corporate growth and change.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the maintenance and improvement of clinical systems to drive process improvement and efficiency.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Embody and demonstrate MapLight’s core values of Integrity, Collaboration, Bravery, and Dedication.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\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 a relevant field or RN; approximately 7+ years in the clinical trial industry with at least 5 years of clinical monitoring including complex therapeutic areas, in-patient trials, and blinded trials. (Recent CNS and/or neuropsychiatry, specifically in-patient schizophrenia and Alzheimer’s disease psychosis experience, strongly preferred.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in small/emerging biotech a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing a clinical monitoring team at a pharmaceutical or biotech company or CRO.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability serve as a role model and mentor to more junior clinical staff.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to build relationships between Investigator sites and MapLight to foster strong collaboration, trust, and positive working relationships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to engage collaboratively with internal and external stakeholders in a professional manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal, oral, and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A self-starter with the ability to work independently and proactively.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to be a “team player” and take on additional responsibilities as requested.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong working knowledge of Good Clinical Practices (GCPs), ALCOA+, and pertinent regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates core understanding of medical terminology and clinical trial activities in relation to execution of a clinical development plan.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High attention to detail and focus on quality and compliance in all aspects of assigned work.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in various clinical software systems (CTMS, eTMF, RIM).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with Word, Excel, PowerPoint, and Microsoft Office.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel independently by air, car and/or train. Location near a major airport preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Position will require up to 30-40% travel with potential to be higher at times of peak study activity. Additional periodic travel for meetings is expected.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$165,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$185,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4016231008,"name":"Clinical Operations","child_ids":[],"parent_id":4064588008}],"offices":[{"id":4012958008,"name":"Remote","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5223207008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4476174008,"location":{"name":"Burlington, MA"},"metadata":null,"id":5223207008,"updated_at":"2026-05-17T21:10:24-04:00","requisition_id":"REG-26-02","title":"Senior Associate, Regulatory Affairs ","company_name":"MapLight Therapeutics","first_published":"2026-05-17T21:10:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Assist Regulatory Lead to support local regulatory activities (e.g., IND/CTA submissions and agency meetings).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide and maintain IND/CTA documentation support in collaboration with Regulatory Lead (e.g., draft and prepare forms and cover letters, liaise with and transfer documents for submissions to/from the publishing vendor or CRO).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain product regulatory information and history documents (e.g., maintain correspondence logs).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Appropriately archive regulatory documents and agency communications.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with CRO’s / partners to support clinical study activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete regulatory forms to support agency communications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide regulatory support through cross-functional interactions in project meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the development and execution of project goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor the development of new regulatory requirements or guidance documents and support Regulatory Lead to advise product teams of the impact on the business or development programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Has flexibility to react rapidly to changing situations/environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willing to travel for occasional in-person team meetings.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Qualifications:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A Bachelor’s degree in a scientific discipline is required. A relevant advanced degree (e.g., MS, PharmD) is preferred and certification is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 2 years in the pharmaceutical industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal, written, and verbal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to understand and communicate scientific/clinical information.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to collaborate with team members to tackle problems and develop a course of action.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong planning and organizing skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to prioritize and balance multiple activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to deal with ambiguity and fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt;This is a hybrid position with three days per week onsite at our office in Burlington, MA or Redwood City, CA.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;MapLight is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$87,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$114,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017894008,"name":"Regulatory","child_ids":[],"parent_id":4064588008}],"offices":[{"id":4012956008,"name":"Burlington","location":"Burlington, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5255575008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4489684008,"location":{"name":"Texas"},"metadata":null,"id":5255575008,"updated_at":"2026-06-11T16:15:15-04:00","requisition_id":"COPS-26-06","title":"Senior Clinical Research Associate (CRA) - Texas or Arizona","company_name":"MapLight Therapeutics","first_published":"2026-06-11T16:15:15-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; This is a remote role located in the Texas OR Arizona region.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel: \u0026lt;/strong\u0026gt;Position will require up to 75% travel with potential to be higher at times of peak activity. Every effort will be made to keep travel regional but travel outside of a region may be required on occasion. Additional periodic travel for meetings is also expected.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;The Sr. CRA will perform quality and compliant Investigator site monitoring and relationship-driven Investigator site management in line with MapLight’s SOPs, our Mission, Vision, and Values, as well as industry quality and regulatory best practices (ICH GCP). The CRA will perform on-site monitoring and centralized monitoring to ensure subject safety, the highest data integrity, and contribute to proactive risk management and inspection readiness.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role will collaborate closely with key cross-functional internal stakeholders including Clinical Operations, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendor partners to ensure quality study oversight from study start up through close out.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;CNS and/or neuropsychiatry, specifically in-patient schizophrenia and/or Alzheimer’s disease psychosis or Alzheimer\u0026#39;s disease agitation experience strongly preferred.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Effectively manage assigned Investigator sites and maintain positive relationships with site personnel.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare for and conduct Pre-Study, Initiation, Interim and Closeout monitoring visits in accordance with MapLight SOPs and procedures, regulatory requirements and industry guidelines and best practices (ICH GCP).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the study team in meeting study milestones (site activation, DSMB meetings, database lock, etc.).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform centralized monitoring activities between on-site visits to ensure timely resolution of action items, oversight of study data quality and flow, and proactively identify and mitigate/manage study risks and issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain quality and compliant documentation related to all aspects of site management including quality and ALCOA+ compliant monitoring visit reports, centralized monitoring reports, site contact reports, Trial Master File/Investigator Site File, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the main MapLight point of contact for Investigator sites to support protocol compliance, streamlined communications, timely responses to site staff needs, and training needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the study team and Investigator sites during inspections or audits, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other assigned tasks, as requested.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the study team(s) in development of study documents and procedures.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;As requested:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the development and maintenance of the study monitoring plan, templates, and tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the set-up, testing, and maintenance of study systems (EDC, eCOA, IRT, etc.) as well as related supporting documents (manuals, eCRF Completion Guidelines, etc.) in collaboration with MapLight and CRO/vendor study team members.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Continually review and reconcile the Trial Master File and Investigator Site File for assigned sites to ensure inspection readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain current knowledge of regulatory requirements and industry best practices related to monitoring, including centralized monitoring and risk-based monitoring.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development and process improvement for the MapLight monitoring function.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development and revision of SOPs, processes, templates, tools, and plans with the aim of continual improvement and streamlining.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the maintenance and improvement of clinical systems to drive process improvement and efficiency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Embody and demonstrate MapLight’s core values of Integrity, Collaboration, Bravery, and Dedication.\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;Approximately 5 plus years in the clinical trial industry with at least 4 years of clinical monitoring experience including complex therapeutic areas, in-patient trials, and blinded trials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;CNS and/or neuropsychiatry, specifically in-patient schizophrenia and/or Alzheimer’s disease psychosis or Alzheimer\u0026#39;s disease agitation experience strongly preferred.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in small/emerging biotech is ideal\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing multiple Investigator sites and multiple studies simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to travel nationally to assigned Investigator sites as needed for required visits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to build relationships between Investigator sites and MapLight to foster strong collaboration, trust, and positive working relationships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong working knowledge of Good Clinical Practices (GCPs), ALCOA+, and pertinent regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to engage collaboratively with internal and external stakeholders in a professional manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal, oral, and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A self-starter with the ability to work independently and proactively.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to be a “team player” and take on additional responsibilities as requested.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates core understanding of medical terminology and clinical trial activities in relation to execution of a clinical development plan.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High attention to detail and focus on quality and compliance in all aspects of assigned work.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in various clinical software systems (EDC, CTMS, eTMF, eCOA, EMR).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with Microsoft Office applications (Word, Excel, PowerPoint, Outlook).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel independently by air, car and/or train. Location near a major airport preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$145,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$160,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4016231008,"name":"Clinical Operations","child_ids":[],"parent_id":4064588008}],"offices":[{"id":4012958008,"name":"Remote","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5210948008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4470117008,"location":{"name":"Burlington, MA"},"metadata":null,"id":5210948008,"updated_at":"2026-05-12T01:00:57-04:00","requisition_id":"COPS-26-04","title":"Senior Clinical Trial Associate (Sr. CTA)","company_name":"MapLight Therapeutics","first_published":"2026-05-05T16:14:15-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Clinical Trial Associate (Sr. CTA) is required to help support Clinical Operations and project teams. The position offers much responsibility and the opportunity to be involved in all phases of the clinical project. The position requires adaptability and the capacity to ‘own’ tasks, problem solve and to see activities through to their end.\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;Interact directly with Clinical (e.g., CRAs, trial managers), site staff, vendors (U.S. and worldwide, as necessary), to provide support in project-specific tasks and the overall management of clinical trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Directly support under the guidance of Operational Leaders, Clinical Leaders, and Clinical Trial Managers. Specific responsibilities include:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain and manage requests for access to and deactivation of study systems users.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinates materials (PowerPoint presentations, templates, outstanding essential document listing, etc.) as needed for internal and external meetings, including requests for materials from external consultants, suppliers, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Distribute safety alerts and relevant documents, if required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain and update study team and vendor contact information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the planning, organizing and execution of study-specific meetings and write and distribute agendas, minutes and regular updates\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May participate in reviewing, formatting and finalizing study-related templates, plans and manuals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with maintaining clinical trial insurance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with questions, issues or requests from the Clinical Research Organization (CRO)/study team and route to the appropriate individual within the organization for resolution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May participate in clinical data review, as required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Responsible for the completeness of documents managed in the Trial Master Files (TMF); performs ongoing reviews of TMF to assure quality of the documentation files and compliance with SOPs and ICH GCP Guidelines\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Route, track and file Clinical documents. May conduct initial/ongoing review of site Clinical regulatory documentation to confirm completeness/track dates and distribute to appropriate team members for review\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain study-related trackers that will support Clinical Operations and individual studies. May analyze or update data associated with the trackers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned to support Study Team Leads and Operational Team Leads\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\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 a relevant subject area is highly recommended or a combination of education and applicable job experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 2+ years in the biotech /pharmaceutical industry /clinical trial management area\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competency of the drug development process with knowledge of ICH-GCP is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal, organizational and planning skills along with excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive and self-starter with the ability to take responsibility for tasks and execute seamlessly. Be able to identify areas for efficiency across studies in the spaces that the position is responsible for.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel up to 35%\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;3 day hybrid in office in Burlington, MA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Maplight is anticipating two Ph2 readouts in Q3 2026\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;MapLight does not accept unsolicited resumes from recruiters, staffing agencies, or search firms.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$115,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$140,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4016231008,"name":"Clinical Operations","child_ids":[],"parent_id":4064588008}],"offices":[{"id":4012956008,"name":"Burlington","location":"Burlington, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5210932008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4470107008,"location":{"name":"Remote"},"metadata":null,"id":5210932008,"updated_at":"2026-06-12T11:11:05-04:00","requisition_id":"COPS-26-03","title":"Senior Specialist, Clinical Business Operations ","company_name":"MapLight Therapeutics","first_published":"2026-05-05T15:55:32-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;MapLight is looking for a dynamic and experienced Senior Specialist, Clinical Business Operations.\u0026amp;nbsp; Reporting to the Executive Director, Clinical Operations, the Senior Specialist will be responsible for supporting all aspects of clinical business operations, including vendor selection, contracts, budget management and performance metrics. The ideal candidate will streamline operational procedures across multiple projects to improve timelines and organization of data.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\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;Vendor selection; including review and analysis, budget negotiations, development, and execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the Request for Proposal (RFP) process. This includes:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work with Clinical Trial Managers (CTM) and Clinical Scientific Leads to develop outsourcing strategy including range of vendors and timelines for award (i.e. schedule a vendor outsourcing strategy meeting).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Use the RFP template to customize to each study.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create a draft of the RFP for review by the study team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate with vendors the RFP timelines and milestones and coordinate feedback to questions/answers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain the internal RFP timelines and milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Following award, be the point of contact to receive the scope of work and budget grid from vendor.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate the review and consolidate the internal study team’s (and finance) questions and comments regarding the budget to the vendor.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate contract review and Coupa entry of budget.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Initiate a warm transfer to the operations team.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage MapLight’s review of all site budgets and contracts. This includes:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead discussions with vendor and CTM to develop study budget and acceptable ranges.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Forecast site contract review timelines as they related to study start up with assistance from the study CTM.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Laise with the Legal Department to ensure MapLight specific site contract template with fall back language is acceptable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with CRO/vendor for process of escalation language to MapLight.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with study team on internal process for triage of contract language and budget requests.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide and/or track contract status updates/reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all executed site contracts are filed in the designated area within MapLight.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with and provide support in developing effective clinical contractual agreements (such as Confidentiality Agreements, Master Services Agreements, Work Orders, Amendments, Change Orders, and any other type of contracts) needed for clinical studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actively managing other clinical financial obligations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate creation and execution of all contract documents and manage the review and negotiation of contract terms and partner in collaboration with Legal, Finance and other internal stakeholders as needed to finalize.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Builds and maintains business relationships and establishes partnerships with CROs, vendors, and other external partners including strategic partnerships and preferred provider relationships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Innovate and maintain tracking systems and metrics, translating complex data into actionable insights for project and program advancement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You can participate and work effectively with multiple cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You have strong interpersonal skills and understand relationships are key to being successful.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You are a leader. Teams love working with you, and you are someone who takes pride in mentoring and supporting the careers of others.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You’re a team player who is willing to roll-up your sleeves and get the job done.\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 or equivalent education required, preferably in Life Sciences, Finance, or Business Administration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A minimum of 3 years experience with outsourcing for clinical trials, vendor negotiations, or operations management, accounting, and finance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with the biotech/pharmaceutical industry at a CRO or sponsor company preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with key Clinical Operations stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and oral communication skills with ability to generate concise reports and verbal updates.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated strong analytical skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated high level of proficiency with Microsoft Office suite (Outlook, Word, Excel, PowerPoint)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be flexible and adaptable to changing project priorities, work assignments and deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;Location: \u0026lt;/strong\u0026gt;This is a remote position.\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;3 day hybrid in office position in Burlington, MA.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;MapLight is anticipating two Ph2 readouts in Q3 2026\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;MapLight does not accept unsolicited resumes from recruiters, staffing agencies, or search firms.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$115,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$135,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4016231008,"name":"Clinical Operations","child_ids":[],"parent_id":4064588008}],"offices":[{"id":4012956008,"name":"Burlington","location":"Burlington, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5025985008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4382628008,"location":{"name":"Remote"},"metadata":null,"id":5025985008,"updated_at":"2026-05-12T01:00:56-04:00","requisition_id":"PV-25-02","title":"Sr. Medical Director, Pharmacovigilance","company_name":"MapLight Therapeutics","first_published":"2025-12-09T17:01:11-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Who We Are: \u0026lt;/strong\u0026gt;MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Medical Director, Pharmacovigilance will lead the medical safety evaluation and benefit-risk assessment for products throughout their lifecycle with focus on patient well-being and compliance and applicable regulatory requirements. This person will lead cross-functional safety management team (SMT) and collaborate with other members Clinical Development and Medical Affairs (CDMA), contract research organizations (CROs), and drug development collaborators/partners to ensure that all clinical safety and benefit-risk assessment is performed adequately for assigned products. Reporting to the Vice President, Pharmacovigilance, the Senior Medical Director will oversee cross-functional teams and may have direct reports\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead product safety surveillance and oversee evolving safety and benefit-risk profiles for assigned products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead cross-functional safety management team (SMT) for assigned products, and responsible for the on-going assessment of benefit-risk profiles and related actions during the product life cycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review safety data from various sources (e.g. pre-clinical, clinical trial data, post-marketing, literature) throughout the development process as well as post marketing for assigned products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for conducting signal detection activities, monitoring, evaluation, interpretation and appropriate management and communication of safety information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent pharmacovigilance on cross-functional product/project teams including review of safety sections of protocols, investigator brochures, informed consent forms, and other documents with safety content.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for strategy and key content of Risk Management documents (DRMPs, RMPs, REMS) and regulatory responses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategy and guidance to safety risk management scientists in writing of periodic reports for assigned products; provide medical interpretation, review and approval.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for up-to-date representation of safety information in Company Core Data Sheet and Investigator Brochure, and other labeling documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform the medical review of all adverse event reports for seriousness, expectedness and causality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coach, mentor and manage safety scientists supporting the surveillance activities for assigned products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Pharmacovigilance function in committees and activities both internally and externally when appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;We consider these behaviors we seek in all ML employees.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;You can participate and work effectively with multiple cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You have strong interpersonal skills and understanding relationships are key to being successful.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You are a leader. Teams love working with you, and you are someone who takes pride in mentoring and supporting the careers of others.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You’re a team player who is willing to roll up your sleeves and get the job done.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;MD or equivalent with 3-5 years of relevant clinical experience\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Preferred: Board Certified/Board Eligible in Neurology or psychiatry\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 10 years’ industry experience, within Drug safety/Pharmacovigilance with investigational and/or marketed products\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Preferred: experience in NDA/IND submissions in neuroscience, psychiatry or neurodegenerative therapeutic area\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience in safety data analysis, signal management, and benefit-risk evaluation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of safety databases (Argus, ArisG/LifeSphere Safety, or similar)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to develop and implement drug safety strategies and risk management plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience with authoring or contributing to clinical study and regulatory submission documents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of relevant local and global regulatory requirements and guidance documents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to lead in a cross functional setting and work collaboratively with internal and external partners in a fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to work within a growing organization and to help the organization evolve over time.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to engage in an open, constructive and continuous dialogue with the Company’s stakeholders based on equality and mutual respect.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective oral and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly motivated, self-driven and dependable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Committed to MapLight\u0026#39;s Core Beliefs and Values.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;This is a remote US position.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel:\u0026lt;/strong\u0026gt; Ability to travel as needed (up to 10%) for corporate and departmental meetings.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;MapLight does not accept unsolicited resumes from recruiters, staffing agencies, or search firms.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD\u0026amp;amp;D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$319,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$361,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017898008,"name":"Pharmacovigilance","child_ids":[],"parent_id":4064588008}],"offices":[{"id":4012956008,"name":"Burlington","location":"Burlington, Massachusetts, United States","child_ids":[],"parent_id":null}]}],"meta":{"total":14}}