{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/entradatherapeutics/jobs/5062031007","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":4597275007,"location":{"name":"Boston, MA"},"metadata":[{"id":17747117007,"name":"Pay transparency","value":{"unit":null,"max_value":"202000.0","min_value":"172000.0"},"value_type":"currency_range"}],"id":5062031007,"updated_at":"2026-04-07T13:54:49-04:00","requisition_id":"89","title":"Associate Director, Drug Substance Development \u0026 Manufacturing ","company_name":"Entrada Therapeutics","first_published":"2026-02-27T10:10:34-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;The Organization\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;What\u0026#39;s happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h2\u0026gt;The Perfect Addition to Our Team\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;You are a motivated, resourceful, and enthusiastic Drug Substance Development \u0026amp;amp; Manufacturing expert excited to support the company at a critical stage in its growth trajectory. You excel at peptide and/or oligonucleotide late-stage process development, GMP manufacturing and supply chain of drug substances. You thrive when performing these activities with minimal supervision in a collaborative matrix environment. At Entrada, you will not be siloed, but rather expected to interact across different functional groups, including Chemistry, Analytical, Drug Product, Quality, and CDMOs. Your ability and desire to thrive in a nimble, fast-paced results-driven environment will set you up for success.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;The Opportunity\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director of Drug Substance Development and Manufacturing will lead and manage late-stage drug substance development for Entrada’s novel pipeline programs. This role will be instrumental in supporting development activities for clinical and commercial batches and ensuring validation parameters for manufacturing batches.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Responsibilities\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Facilitate timely execution, disposition, and release of intermediate/drug substance batches through detailed technical review of master batch records, executed batch records and other cGMP documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with internal and external Quality Assurance, Quality Control and Technical Operations teams to execute late-stage development activities such as Process Characterization and Process Performance Qualifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a person-in-plant for smooth execution of critical manufacturing activities for clinical and commercial batches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct risk assessments and develop mitigation strategies for manufacturing-related issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and resolve manufacturing issues and escalate appropriately to internal and/or joint governance if required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement and manage the Continuous Process Verification (CPV) program to ensure manufacturing process remain in a constant state of control and meet validated parameters.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author/review change controls to introduce process improvements through the lifecycle of programs from Phase 1 through Phase 3/validation and commercialization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with other internal functions including chemistry, analytical, quality control, quality assurance, DP, and regulatory affairs to ensure programs are effectively supported and high-quality standard maintained.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Entrada team for CDMO due diligence during new CDMO selection to vet capabilities, risks and investments required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author/review related sections in regulatory filing documents (IND, IMPD, NDA, BLA, MAA, etc.).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other tasks as assigned or as required for a given program.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;The Necessities\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;At Entrada, our passion for science, our devotion to patients and our values drives our\u0026amp;nbsp;behavior:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Humanity\u0026lt;/strong\u0026gt; - We genuinely care about patients and about one another.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Tenacity\u0026lt;/strong\u0026gt; - We are relentless and persistent in the pursuit of developing therapies\u0026amp;nbsp;for patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Creativity\u0026lt;/strong\u0026gt; - We are creative problem solvers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Collaboration\u0026lt;/strong\u0026gt; - We are more than the sum of our parts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Curiosity\u0026lt;/strong\u0026gt; - We have a growth mindset and push conventional thought and theory.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;To thrive on our team, you will need to come with:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Master’s or suitable advanced degree in organic chemistry or other scientific or engineering discipline with 8+ years of related experience in pharmaceutical industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated proficiency in process development, tech transfer, scale-up, GMP manufacturing DS for clinical, and commercial supplies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in managing activities and resolving manufacturing challenges at CDMOs during routine cGMP manufacturing and process validations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experienced in onboarding/managing/collaborating with CDMOs, raw material suppliers, testing partners, and other production partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience in SPPS/SPOS, downstream purification and lyophilization is highly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to develop and maintain production timelines and budgets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Up-to-date with industry practices and regulations (e.g. GxP, ISO, ICH, etc.) across multiple health authorities (e.g. FDA and EMA).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interpret and relate Quality standards for implementation and review.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management, interpersonal, communication, and problem-solving skills preferable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to communicate clearly and professionally both in writing and verbally.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel up to 20% (domestic and international).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This is a US based remote position with preference given to local New England based candidates. This role will require minimum monthly or quarterly travel to the Entrada Therapeutics Headquarters located in Boston, MA.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;What We Offer: Meaningful Work, Fair Rewards, and Real Support\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;At Entrada Therapeutics, we understand that compensation and total rewards are a major consideration when exploring a new opportunity. We believe in transparency and equity and are committed to sharing salary ranges for every position, along with insight into our compensation philosophy, in accordance with certain state requirements in the United States and fostering a fair and open environment at the onset.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;But we also know it is more than just pay. When you join Entrada, you’ll be part of a mission-driven team with access to comprehensive health, dental and vision coverage; life and disability insurance; with a 401(k) match. We pride ourselves on offering competitive benefits that empower our employees and reflect the value of their contributions – offering paid, gender-inclusive parental leave, holistic support for your health and well-being, education reimbursement, discretionary time off and commuting benefits aligned to your working model. If you find yourself working from our office in Boston’s Seaport District, this puts you steps away from some of the best the city has to offer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;“Our approach to compensation is grounded in transparency, equity and performance for the unique contributions each person brings. At Entrada, we know that meaningful work deserves meaningful reward — and we view compensation as one way we show appreciation for the collaboration, curiosity and commitment that drive our mission forward.”\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;— Kerry Robert, SVP of People\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The salary for this opportunity ranges from $172,000-$202,000 The final base compensation offered will depend on several considerations which include but may not be limited to a candidate’s skills, competencies, experience and other job-related factors permitted by law. The final salary offered may fall outside of this range. \u0026lt;span style=\u0026quot;color: rgb(255, 255, 255);\u0026quot;\u0026gt;#LI-JF1 #LI-Remote\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;Equal Opportunity Employer\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Third Party Staffing Agencies\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Privacy Statement\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics, Inc. (the “\u0026lt;strong\u0026gt;Entrada\u0026lt;/strong\u0026gt;,” “\u0026lt;strong\u0026gt;we,\u0026lt;/strong\u0026gt;” “\u0026lt;strong\u0026gt;us,\u0026lt;/strong\u0026gt;” or “\u0026lt;strong\u0026gt;our\u0026lt;/strong\u0026gt;”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement \u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.entradatx.com/privacy-notice\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;here \u0026lt;/strong\u0026gt;\u0026lt;/a\u0026gt;\u0026lt;/span\u0026gt;to understand how and when your data is being used.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4036127007,"name":"Technical Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4026254007,"name":"Boston, MA","location":"Boston, Massachusetts, United States","child_ids":[4027822007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/entradatherapeutics/jobs/5109377007","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":4618824007,"location":{"name":"Boston, MA"},"metadata":[{"id":17747117007,"name":"Pay transparency","value":{"unit":"USD","max_value":"204000.0","min_value":"171000.0"},"value_type":"currency_range"}],"id":5109377007,"updated_at":"2026-04-15T16:43:25-04:00","requisition_id":"106","title":"Associate Director, Regulatory Affairs","company_name":"Entrada Therapeutics","first_published":"2026-04-15T16:18:16-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;The Organization\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;What\u0026#39;s happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h2\u0026gt;The Perfect Addition to Our Team\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;You are passionate and dedicated to your work, with a commitment to overcome challenges and deliver on our potential to develop transformative therapies for patients and their caregivers. You bring energy and enthusiasm to your role, while recognizing that a steady and consistent effort is required to successfully develop novel medicines.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;The Opportunity\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;The Regulatory Affairs team at Entrada is a dynamic, growing team. The Associate Director will support global regulatory activities for Entrada’s pipeline, with a focus on clinical-stage assets. Reporting to the Senior Vice President, Regulatory Affairs, the ideal candidate will collaborate with cross-functional teams to efficiently advance the global development of genetic medicines for rare and serious unmet medical needs. This high-impact role will be critical to the success of the Regulatory department and Entrada’s mission to discover, develop and commercialize life-changing medicines that are safe, effective and accessible to those who need them.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Responsibilities\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the global regulatory strategy for multiple clinical stage programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner on the development, preparation, and timely completion of health authority submissions, including the authoring, submission, and archiving for IND, CTA, and EU-CTR submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop strong working relationships with Regulatory colleagues and cross-functional project teams to support achievement of timelines and portfolio deliverables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain strong relationships and communication with external stakeholders, including regulatory agencies, CROs, CDMOs, consulting groups, and other third parties.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with various departments including Nonclinical, Quality, Manufacturing, and Clinical to maximize opportunities while ensuring alignment with regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead or contribute to the development and review of procedures and work instructions aligned with GxPs, Guidance, industry standards, and corporate objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in study team meetings, providing updates and addressing questions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify opportunities and risks within our Regulatory department and the development programs, and support approaches to mitigate and resolve risks.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;The Necessities\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;At Entrada, our passion for science, our devotion to patients and our values drives our\u0026amp;nbsp;behavior:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Humanity\u0026lt;/strong\u0026gt; - We genuinely care about patients and about one another.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Tenacity\u0026lt;/strong\u0026gt; - We are relentless and persistent in the pursuit of developing therapies\u0026amp;nbsp;for patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Creativity\u0026lt;/strong\u0026gt; - We are creative problem solvers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Collaboration\u0026lt;/strong\u0026gt; - We are more than the sum of our parts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Curiosity\u0026lt;/strong\u0026gt; - We have a growth mindset and push conventional thought and theory.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;To thrive on our team, you will need to come with:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS or MS with at least 6+ years of increasing responsibility in Regulatory Affairs; an advanced degree, RAC, or education in a scientific field preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A demonstrated record of accomplishment, including support and execution of both US and global regulatory strategies (ie, with IND, CTA, CTR, NDA, BLA, and/or MAA activities).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of the drug development process, GxP regulations, ICH, and FDA Guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with rare diseases, pediatrics, genetic medicines, or leveraging expedited development pathways (eg, accelerated approval) is strongly preferred; experience with neuromuscular or ocular therapeutic areas is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A strong work ethic, excellent verbal and written communication skills, and a desire to work collaboratively with matrixed project teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational skills and the ability to work on multiple projects with tight timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A motivated and driven attitude, with a proactive work style and a results-oriented mindset.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Integrity, a desire to learn and grow, and a commitment to excellence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This is a US based remote position, with preference given to local New England based candidates. This role will require minimum quarterly travel to the Entrada Therapeutics Headquarters located in Boston, MA\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;What We Offer: Meaningful Work, Fair Rewards, and Real Support\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;At Entrada Therapeutics, we understand that compensation and total rewards are a major consideration when exploring a new opportunity. We believe in transparency and equity and are committed to sharing salary ranges for every position, along with insight into our compensation philosophy, in accordance with certain state requirements in the United States and fostering a fair and open environment at the onset.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;But we also know it is more than just pay. When you join Entrada, you’ll be part of a mission-driven team with access to comprehensive health, dental and vision coverage; life and disability insurance; with a 401(k) match. We pride ourselves on offering competitive benefits that empower our employees and reflect the value of their contributions – offering paid, gender-inclusive parental leave, holistic support for your health and well-being, education reimbursement, discretionary time off and commuting benefits aligned to your working model. If you find yourself working from our office in Boston’s Seaport District, this puts you steps away from some of the best the city has to offer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;“Our approach to compensation is grounded in transparency, equity and performance for the unique contributions each person brings. At Entrada, we know that meaningful work deserves meaningful reward — and we view compensation as one way we show appreciation for the collaboration, curiosity and commitment that drive our mission forward.”\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;— Kerry Robert, SVP of People\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The salary for this opportunity ranges from $171,000-$204,000. The final base compensation offered will depend on several considerations which include but may not be limited to a candidate’s skills, competencies, experience and other job-related factors permitted by law. The final salary offered may fall outside of this range. \u0026lt;span style=\u0026quot;color: rgb(255, 255, 255);\u0026quot;\u0026gt;#LI-GG1 #LI-Remote\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;Equal Opportunity Employer\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Third Party Staffing Agencies\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Privacy Statement\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics, Inc. (the “\u0026lt;strong\u0026gt;Entrada\u0026lt;/strong\u0026gt;,” “\u0026lt;strong\u0026gt;we,\u0026lt;/strong\u0026gt;” “\u0026lt;strong\u0026gt;us,\u0026lt;/strong\u0026gt;” or “\u0026lt;strong\u0026gt;our\u0026lt;/strong\u0026gt;”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement \u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.entradatx.com/privacy-notice\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;here \u0026lt;/strong\u0026gt;\u0026lt;/a\u0026gt;\u0026lt;/span\u0026gt;to understand how and when your data is being used.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4039246007,"name":"Regulatory Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4026254007,"name":"Boston, MA","location":"Boston, Massachusetts, United States","child_ids":[4027822007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/entradatherapeutics/jobs/5077431007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4604367007,"location":{"name":"Boston, MA"},"metadata":[{"id":17747117007,"name":"Pay transparency","value":{"unit":null,"max_value":"335000.0","min_value":"292000.0"},"value_type":"currency_range"}],"id":5077431007,"updated_at":"2026-04-07T13:54:49-04:00","requisition_id":"104","title":"Executive Director, Investor Relations","company_name":"Entrada Therapeutics","first_published":"2026-03-12T13:12:05-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;The Organization\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;What\u0026#39;s happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h2\u0026gt;The Perfect Addition to Our Team\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;You are intellectually curious and can bring new ideas and perspectives to lead the development, implementation, and management of our investor relations function. You follow up and follow through, efficiently connecting problems with solutions. You work successfully in a fast-paced team environment and have strong interpersonal skills, effectively building working relationships with leaders across the Company and with outside parties.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;The Opportunity\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;The Executive Director, Investor Relations will be responsible for developing and executing a comprehensive investor relations strategy that enhances Entrada’s visibility, credibility, and positioning within the financial community and broader stakeholder landscape. Reporting to the Chief Financial Officer, the ideal candidate will combine deep investor relations and financial expertise with strong scientific and clinical fluency to build investor confidence, drive awareness, and support long-term shareholder value creation for a NASDAQ-listed biotechnology company with an expanding portfolio of clinical-stage programs.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Responsibilities\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Drive the strategic direction, planning, and execution of the investor relations function, including financial communications, while building and continuously strengthening a best-in-class investor relations program.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a trusted advisor to senior leadership by providing insight and guidance on investor messaging, communications effectiveness, market dynamics, and investor sentiment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as the primary point of contact to the investment community, responding to external inquiries in an accurate, appropriate, and timely manner; establish and maintain strong relationships with biotechnology-focused buy-side and sell-side analysts and institutional investors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain proactive engagement with investors and analysts to clearly communicate the Company’s long-term vision, clinical and platform strategy, differentiation, opportunity, risk factors, and key milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the development and coordination of financial and investor communications—including earnings releases, investor webcasts, investor presentations, Company corporate presentations and investor relations section of the Company website\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate cross-functionally with Finance and Legal to support the timely and compliant execution of external financial disclosures and investor communications including periodic reports (Form 10-K and Form 10-Q), annual proxy statements and other reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the Company’s participation in investment community events, including investor conferences, non-deal roadshows, analyst days, and targeted investor meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, track, and report key investor relations metrics in our Irwin investor relations system to assess program effectiveness and inform continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor published research analyst reports covering the Company and analyze biopharmaceutical industry trends, investor perceptions, and competitor communications to inform strategic positioning and messaging.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support capital markets activities, including potential financings and strategic transactions, in close partnership with the CFO and senior leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with the Chief Corporate Affairs Officer to ensure alignment with the broader corporate communications strategy and Entrada brand.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage external agencies and vendors, as needed, ensuring high-quality deliverables and disciplined management of external spend.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all investor communications and activities fully comply with SEC regulations and disclosure requirements, including Regulation FD and NASDAQ listing standards.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;The Necessities\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;At Entrada, our passion for science, our devotion to patients and our values drives our\u0026amp;nbsp;behavior:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Humanity\u0026lt;/strong\u0026gt; - We genuinely care about patients and about one another.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Tenacity\u0026lt;/strong\u0026gt; - We are relentless and persistent in the pursuit of developing therapies\u0026amp;nbsp;for patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Creativity\u0026lt;/strong\u0026gt; - We are creative problem solvers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Collaboration\u0026lt;/strong\u0026gt; - We are more than the sum of our parts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Curiosity\u0026lt;/strong\u0026gt; - We have a growth mindset and push conventional thought and theory.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;To thrive on our team, you will need to come with:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; advanced degree (PhD, MD, MBA, or MS in life sciences, biotechnology, or finance-related discipline) preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of progressive experience in investor relations within the biotechnology or pharmaceutical industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting investor relations for a publicly traded biotechnology or pharmaceutical company, preferably NASDAQ-listed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in a clinical-stage or pre-commercial biotechnology environment strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Established relationships within the biotechnology buy-side and sell-side community strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to develop and execute investor relations strategies that effectively reach and influence target audiences.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong financial acumen and financial modeling familiarity, with the ability to clearly communicate complex financial and clinical information to diverse external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop clear and compelling PowerPoint presentations for earnings calls, investor meetings, and board discussions that translate complex financial and strategic information into concise, visually compelling narratives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience supporting equity offerings, capital markets transactions, or other strategic financings preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead the use of investor relations software solutions to support investor engagement, shareholder monitoring and analytics, Irwin experience preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills, with exceptional attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly self-directed with exceptional project management and organizational skills, and the ability to prioritize multiple high-impact workstreams and deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience building, managing, and scaling investor relations capabilities across internal teams and external partners (e.g., agencies, vendors, consultants).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to work collaboratively and influence across functions and with senior executives to support the achievement of business objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of the drug development lifecycle and the regulatory and disclosure environment for biopharmaceutical companies, including SEC and Regulation FD requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience preparing senior executives and Board members for investor engagement and earnings communications preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel approximately 25% as required to support investor engagement and key industry events.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This is a US based remote position, with preference given to local New England based candidates who can be in office 1 day per week to the Entrada Therapeutics Headquarters located in Boston, MA.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;What We Offer: Meaningful Work, Fair Rewards, and Real Support\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;At Entrada Therapeutics, we understand that compensation and total rewards are a major consideration when exploring a new opportunity. We believe in transparency and equity and are committed to sharing salary ranges for every position, along with insight into our compensation philosophy, in accordance with certain state requirements in the United States and fostering a fair and open environment at the onset.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;But we also know it is more than just pay. When you join Entrada, you’ll be part of a mission-driven team with access to comprehensive health, dental and vision coverage; life and disability insurance; with a 401(k) match. We pride ourselves on offering competitive benefits that empower our employees and reflect the value of their contributions – offering paid, gender-inclusive parental leave, holistic support for your health and well-being, education reimbursement, discretionary time off and commuting benefits aligned to your working model. If you find yourself working from our office in Boston’s Seaport District, this puts you steps away from some of the best the city has to offer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;“Our approach to compensation is grounded in transparency, equity and performance for the unique contributions each person brings. At Entrada, we know that meaningful work deserves meaningful reward — and we view compensation as one way we show appreciation for the collaboration, curiosity and commitment that drive our mission forward.”\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;— Kerry Robert, SVP of People\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The salary for this opportunity ranges from $292,000-$335,000. The final base compensation offered will depend on several considerations which include but may not be limited to a candidate’s skills, competencies, experience and other job-related factors permitted by law. The final salary offered may fall outside of this range.\u0026lt;span style=\u0026quot;color: rgb(255, 255, 255);\u0026quot;\u0026gt;#LI-GG1 #LI-Remote\u0026lt;/span\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;Equal Opportunity Employer\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Third Party Staffing Agencies\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Privacy Statement\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics, Inc. (the “\u0026lt;strong\u0026gt;Entrada\u0026lt;/strong\u0026gt;,” “\u0026lt;strong\u0026gt;we,\u0026lt;/strong\u0026gt;” “\u0026lt;strong\u0026gt;us,\u0026lt;/strong\u0026gt;” or “\u0026lt;strong\u0026gt;our\u0026lt;/strong\u0026gt;”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement \u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.entradatx.com/privacy-notice\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;here \u0026lt;/strong\u0026gt;\u0026lt;/a\u0026gt;\u0026lt;/span\u0026gt;to understand how and when your data is being used.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4036132007,"name":"Finance","child_ids":[],"parent_id":null}],"offices":[{"id":4026254007,"name":"Boston, MA","location":"Boston, Massachusetts, United States","child_ids":[4027822007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/entradatherapeutics/jobs/5132958007","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":4630038007,"location":{"name":"Boston, MA"},"metadata":[{"id":17747117007,"name":"Pay transparency","value":{"unit":null,"max_value":"166000.0","min_value":"127000.0"},"value_type":"currency_range"}],"id":5132958007,"updated_at":"2026-05-08T13:08:22-04:00","requisition_id":"109","title":"Manager, Market Intelligence and Strategy","company_name":"Entrada Therapeutics","first_published":"2026-05-08T13:08:22-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;The Organization\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;What\u0026#39;s happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h2\u0026gt;The Perfect Addition to Our Team\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;You are interested in working at the intersection of life sciences and business. You want to join a high growth biotech company in a business strategy role to help support the team by synthesizing and communicating strategic insights from market and competitor developments. You bring to the table the combination of an inquisitive spirit, critical thinking, and analytical skills. You love following innovative science, performing data-driven analyses and contributing strategic insights. You thrive in figuring out the details and understanding the nuances while still making connections to the bigger picture. You look forward to working with and learning from cross-functional leaders across the organization while helping shape long-term strategy\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;The Opportunity\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;This individual will lead and support many different aspects of competitive and market intelligence to support new product planning. Example workstreams include competitive monitoring and tracking, conference coverage, and strategy development. The ideal candidate will conduct primary and secondary research to gather market insights and data and use them to inform analysis and planning implications. This individual will be expected to lead the Competitive Intelligence workstream and distill market insights and data in a timely manner to create concise summaries for internal communications. They will also support various strategic workstreams by conducting focused evaluations of market trends and supporting commercial assessments to help drive recommendations.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Responsibilities\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Competitive Landscape\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead competitive intelligence activities, including tracking, analyzing, synthesizing, and communicating competitor and industry activity across key stakeholders (Strategy, Regulatory Affairs, Medical Affairs, Clinical Development, Clinical Operations, and Business Development).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor industry activity and emerging trends through conference coverage and external intelligence to inform internal decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Market Insights\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Gather, analyze, and synthesize market data to support data-driven insights and timely communication to internal stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and execute cross-functional primary market research, partnering with internal teams to define objectives, methodologies, and select vendors (HCPs, KOLs, patients, payers, and advanced analytics partners).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate market research, claims analysis, and payer insights into early go-to-market strategy and commercialization readiness.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;New Product Planning\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Monitor and routinely update competitor pipeline and strategic direction to inform forward-looking internal program strategy, positioning, and planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify gaps and opportunities within the evolving landscape to support early commercial strategy development, including treatment positioning, segmentation, pricing scenarios, and foundational launch assumptions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely present insights and strategic recommendations to senior leadership and cross-functional leadership teams to inform decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop investor- and Board-facing slide decks that articulate competitive differentiation and strategic positioning.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;The Necessities\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;At Entrada, our passion for science, our devotion to patients and our values drives our\u0026amp;nbsp;behavior:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Humanity\u0026lt;/strong\u0026gt; - We genuinely care about patients and about one another.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Tenacity\u0026lt;/strong\u0026gt; - We are relentless and persistent in the pursuit of developing therapies\u0026amp;nbsp;for patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Creativity\u0026lt;/strong\u0026gt; - We are creative problem solvers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Collaboration\u0026lt;/strong\u0026gt; - We are more than the sum of our parts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Curiosity\u0026lt;/strong\u0026gt; - We have a growth mindset and push conventional thought and theory.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;To thrive on our team, you will need to come with:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor of Science or Arts degree in life sciences (biology, biochemistry, chemistry, etc.) required; advanced degree preferred (PhD, MS, or equivalent).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;4+ years of experience in biotech/pharma in roles such as competitive intelligence, market insights, or management consulting with a life sciences focus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong scientific literacy with the ability to interpret clinical and preclinical data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience synthesizing and communicating accurate, timely competitive insights on drug development / corporate strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in designing and conducting interviews with external experts or KOLs is strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills, with the ability to synthesize complex information into clear recommendations and present insights effectively using Microsoft PowerPoint and Excel.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently in a fast-paced, innovative, and collaborative environment, with a strong team-oriented mindset, can-do attitude, and flexibility to adapt based on new insights and team input.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This position is a US remote-based position requiring a minimum of 1-2 days per week onsite at the Entrada Therapeutics Headquarters in Boston, MA.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;What We Offer: Meaningful Work, Fair Rewards, and Real Support\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;At Entrada Therapeutics, we understand that compensation and total rewards are a major consideration when exploring a new opportunity. We believe in transparency and equity and are committed to sharing salary ranges for every position, along with insight into our compensation philosophy, in accordance with certain state requirements in the United States and fostering a fair and open environment at the onset.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;But we also know it is more than just pay. When you join Entrada, you’ll be part of a mission-driven team with access to comprehensive health, dental and vision coverage; life and disability insurance; with a 401(k) match. We pride ourselves on offering competitive benefits that empower our employees and reflect the value of their contributions – offering paid, gender-inclusive parental leave, holistic support for your health and well-being, education reimbursement, discretionary time off and commuting benefits aligned to your working model. If you find yourself working from our office in Boston’s Seaport District, this puts you steps away from some of the best the city has to offer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;“Our approach to compensation is grounded in transparency, equity and performance for the unique contributions each person brings. At Entrada, we know that meaningful work deserves meaningful reward — and we view compensation as one way we show appreciation for the collaboration, curiosity and commitment that drive our mission forward.”\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;— Kerry Robert, SVP of People\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The salary for this opportunity ranges from$127,000-$166,000. The final base compensation offered will depend on several considerations which include but may not be limited to a candidate’s skills, competencies, experience and other job-related factors permitted by law. The final salary offered may fall outside of this range. \u0026lt;span style=\u0026quot;color: rgb(255, 255, 255);\u0026quot;\u0026gt;#LI-Remote #LI-GG1\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;Equal Opportunity Employer\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Third Party Staffing Agencies\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Privacy Statement\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics, Inc. (the “\u0026lt;strong\u0026gt;Entrada\u0026lt;/strong\u0026gt;,” “\u0026lt;strong\u0026gt;we,\u0026lt;/strong\u0026gt;” “\u0026lt;strong\u0026gt;us,\u0026lt;/strong\u0026gt;” or “\u0026lt;strong\u0026gt;our\u0026lt;/strong\u0026gt;”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement \u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.entradatx.com/privacy-notice\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;here \u0026lt;/strong\u0026gt;\u0026lt;/a\u0026gt;\u0026lt;/span\u0026gt;to understand how and when your data is being used.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4042928007,"name":"Other R\u0026D","child_ids":[],"parent_id":null}],"offices":[{"id":4026254007,"name":"Boston, MA","location":"Boston, Massachusetts, United States","child_ids":[4027822007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/entradatherapeutics/jobs/5162033007","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":4644288007,"location":{"name":"Boston, MA"},"metadata":[{"id":17747117007,"name":"Pay transparency","value":{"unit":null,"max_value":"0.0","min_value":"0.0"},"value_type":"currency_range"}],"id":5162033007,"updated_at":"2026-06-12T10:40:55-04:00","requisition_id":"112","title":"Part Time Study Manager (CONTRACT)","company_name":"Entrada Therapeutics","first_published":"2026-06-12T10:40:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;The Organization\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;What\u0026#39;s happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h2\u0026gt;The Opportunity\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;We are seeking an experienced part‑time Contract Study Manager to support unblinded clinical trial operations across one or more ongoing studies. This role is ideal for a seasoned clinical operations professional who can independently manage unblinded workflows, maintain strict separation from blinded teams, and ensure operational excellence in a fast‑moving environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The contractor will oversee day‑to‑day unblinded activities, including vendor coordination, drug supply workflows, unblinded data review, and operational documentation. This role requires exceptional judgment, attention to detail, and comfort working with sensitive information.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Responsibilities\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the unblinded operational lead for assigned clinical studies, ensuring all activities are conducted in compliance with ICH/GCP, regulatory requirements, and internal procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and manage various study activities, including CROs, country and site selection, informed consent development and maintenance, eCRF design and implementation, protocols, study plans and manuals, IBs, CSRs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee study documentation, including study plans, logs, trackers, and training materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support data review, reconciliation, and issue resolution in collaboration with Data Management, Biostatistics, and Safety teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain appropriate firewalls between blinded and unblinded personnel, ensuring study integrity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide unblinded operational updates to internal stakeholders while safeguarding treatment‑related information.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify and support resolution/escalation of trial conduct-related issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in cross‑functional meetings as the unblinded representative, escalating risks and proposing mitigation strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support components of site start‑up, ongoing monitoring, and closeout activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to inspection readiness and support regulatory or QA requests related to unblinded processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide flexible support aligned with study needs, including availability during key milestones (e.g., dose escalations, interim analyses, database locks).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;The Necessities\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;At Entrada, our passion for science, our devotion to patients and our values drives our\u0026amp;nbsp;behavior:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Humanity\u0026lt;/strong\u0026gt; - We genuinely care about patients and about one another.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Tenacity\u0026lt;/strong\u0026gt; - We are relentless and persistent in the pursuit of developing therapies\u0026amp;nbsp;for patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Creativity\u0026lt;/strong\u0026gt; - We are creative problem solvers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Collaboration\u0026lt;/strong\u0026gt; - We are more than the sum of our parts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Curiosity\u0026lt;/strong\u0026gt; - We have a growth mindset and push conventional thought and theory.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;To thrive on our team, you will need to come with:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BA/BS degree with 7+ years of clinical operations experience, including direct involvement in unblinded or partially blinded study management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong working knowledge of ICH/GCP, clinical trial conduct, and regulatory expectations within global clinical trials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience in the drug development process, including trial design, trial planning and management, and CRO and vendor oversight.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills and proven ability to work effectively across functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized, detail‑oriented, and able to work independently in a contract capacity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with EU‑CTR is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel occasionally for key meetings or site visits, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Preference for candidates based in the New England region.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This is a part-time contract, US based remote position, with preference given to local New England based candidates. \u0026lt;span style=\u0026quot;color: rgb(255, 255, 255);\u0026quot;\u0026gt;#LI-JF1 #LI-Remote\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;Equal Opportunity Employer\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Third Party Staffing Agencies\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Privacy Statement\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics, Inc. (the “\u0026lt;strong\u0026gt;Entrada\u0026lt;/strong\u0026gt;,” “\u0026lt;strong\u0026gt;we,\u0026lt;/strong\u0026gt;” “\u0026lt;strong\u0026gt;us,\u0026lt;/strong\u0026gt;” or “\u0026lt;strong\u0026gt;our\u0026lt;/strong\u0026gt;”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement \u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.entradatx.com/privacy-notice\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;here \u0026lt;/strong\u0026gt;\u0026lt;/a\u0026gt;\u0026lt;/span\u0026gt;to understand how and when your data is being used.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4059274007,"name":"Clinical Operations \u0026 Biometrics","child_ids":[],"parent_id":null}],"offices":[{"id":4026254007,"name":"Boston, MA","location":"Boston, Massachusetts, United States","child_ids":[4027822007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/entradatherapeutics/jobs/5155427007","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":4641071007,"location":{"name":"Boston, MA"},"metadata":[{"id":17747117007,"name":"Pay transparency","value":{"unit":null,"max_value":"0.0","min_value":"0.0"},"value_type":"currency_range"}],"id":5155427007,"updated_at":"2026-06-04T09:29:56-04:00","requisition_id":"111","title":"Senior Clinical Trial Associate (CONTRACT)","company_name":"Entrada Therapeutics","first_published":"2026-06-04T09:29:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;The Organization\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;What\u0026#39;s happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h2\u0026gt;The Perfect Addition to Our Team\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;You are patient focused and excited about the opportunity to help support and develop the Clinical Operations organization at Entrada. You enjoy a fast-paced environment and juggling competing priorities. You follow up and follow through, connecting problems with solutions efficiently. You work successfully in a team environment with strong interpersonal skills to effectively build working relationships inside and outside the company.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;The Opportunity\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;This individual will assist the clinical operations team in the day-to-day operations, study start up and set-up, execution, and closeout of assigned trials.\u0026amp;nbsp; The individual is accountable to the clinical trial team for the support of trial execution and works collaboratively with cross-functional team members and vendors to ensure proper set-up of trial processes and plans to execute the protocol in accordance with established SOPs and standards.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Responsibilities\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the day-to-day operations of assigned trials to ensure completion per established project team goals and objectives in compliance with ICH/GCP guidelines, from study start-up to close-out.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides accurate and up-to date clinical trial information within relevant tracking tools and provides regular updates of trial progression to the clinical trial team, including those related to protocol deviations, adverse events, and site personnel trainings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the development of trial related plans and manuals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures timely maintenance of the TMF, filing and reconciliation according to regulatory guidance and internal SOPs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participates and ensures appropriate documentation of clinical team meetings, including meeting minutes, agendas, and action items.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage vendor POs and trial payments (including budget reconciliation), including invoice review and approval.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the set-up and management of clinical trial supplies and biosample management where needed (drug product, ancillary and other).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in external training activities (suppliers, clinical sites etc.).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the management of trial completion activities, including data review, database lock and trial closeout.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;The Necessities\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;At Entrada, our passion for science, our devotion to patients and our values drives our\u0026amp;nbsp;behavior:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Humanity\u0026lt;/strong\u0026gt; - We genuinely care about patients and about one another.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Tenacity\u0026lt;/strong\u0026gt; - We are relentless and persistent in the pursuit of developing therapies\u0026amp;nbsp;for patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Creativity\u0026lt;/strong\u0026gt; - We are creative problem solvers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Collaboration\u0026lt;/strong\u0026gt; - We are more than the sum of our parts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Curiosity\u0026lt;/strong\u0026gt; - We have a growth mindset and push conventional thought and theory.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;To thrive on our team, you will need to come with:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BA/BS degree with at least 2+ years of relevant experience in clinical operations working at a biotech or pharmaceutical company.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of clinical trial operations, including all phases from study start-up to close-out.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and take initiative on projects under minimal supervision.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;General working knowledge of drug development and ICH/GCP guidelines is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous CRO or vendor management experience preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, written, administrative, and computer skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills with a strong attention for detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel approximately 5% of the time, as determined by the needs of the business.\u0026amp;nbsp;\u0026lt;span style=\u0026quot;color: rgb(255, 255, 255);\u0026quot;\u0026gt;#LI-Remote #LI-JF1\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This role is a long-term contract position that follows a remote working model, requiring monthly or quarterly travel to the Entrada Therapeutics Headquarters in Boston, MA.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;Equal Opportunity Employer\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Third Party Staffing Agencies\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Privacy Statement\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics, Inc. (the “\u0026lt;strong\u0026gt;Entrada\u0026lt;/strong\u0026gt;,” “\u0026lt;strong\u0026gt;we,\u0026lt;/strong\u0026gt;” “\u0026lt;strong\u0026gt;us,\u0026lt;/strong\u0026gt;” or “\u0026lt;strong\u0026gt;our\u0026lt;/strong\u0026gt;”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement \u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.entradatx.com/privacy-notice\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;here \u0026lt;/strong\u0026gt;\u0026lt;/a\u0026gt;\u0026lt;/span\u0026gt;to understand how and when your data is being used.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4059274007,"name":"Clinical Operations \u0026 Biometrics","child_ids":[],"parent_id":null}],"offices":[{"id":4026254007,"name":"Boston, MA","location":"Boston, Massachusetts, United States","child_ids":[4027822007],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/entradatherapeutics/jobs/5141480007","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":4634167007,"location":{"name":"Boston, MA"},"metadata":[{"id":17747117007,"name":"Pay transparency","value":{"unit":null,"max_value":"0.0","min_value":"0.0"},"value_type":"currency_range"}],"id":5141480007,"updated_at":"2026-05-19T11:13:28-04:00","requisition_id":"110","title":"Senior Patient Recruitment and Retention Lead (CONTRACT)","company_name":"Entrada Therapeutics","first_published":"2026-05-19T10:27:48-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;The Organization\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;What\u0026#39;s happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h2\u0026gt;The Perfect Addition to Our Team\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;You are a seasoned leader in the pharmaceutical industry who is eager to shape and implement patient recruitment and retention strategies for clinical trials. You are well organized and collaborative, able to work seamlessly with teams to drive our clinical activities. You thrive in a fast-paced environment, juggling priorities, and stepping in wherever needed. With a proven track record in scaling operations within biotech or pharmaceutical settings, you are a results-driven problem solver who efficiently connects problems with solutions.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;The Opportunity\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;The Patient Recruitment \u0026amp;amp; Retention Contractor will be responsible for development and execution of Entrada’s clinical trial recruitment and retention, bringing proven expertise in building and optimizing clinical trials, feasibility, patient recruitment, and regulatory compliance. This role reports to the SVP, Clinical and Business Operations \u0026amp;amp; Quantitative Science, and will support ongoing and new global rare disease trials.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Responsibilities\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In partnership with study teams, develop and oversee global patient recruitment and retention strategies across all clinical programs, ensuring alignment with portfolio timelines, program priorities, and corporate development goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive execution of integrated feasibility strategies, including landscape analysis, enrollment modeling, and site capability assessments to inform protocol optimization and accelerate trial start up.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure alignment between ongoing trial feasibility efforts and patient recruitment and retention strategies through effective vendor partnerships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and monitor enrollment KPIs and recruitment progress; providing regular progress reporting to Clinical Operations leadership and study teams as well as senior leadership, implementing course corrections when needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as subject matter expert on global regulatory expectations (FDA, EMA) for diversity and inclusive research practices, supporting cross-functional teams on compliance and strategies and staying up-to-date on recruitment technologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bring the patient voice and experience into the patient recruitment and retention strategy and related materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify risks to enrollment timelines, implementing mitigation strategies where necessary and communicating said risks to study leadership teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide insights to program-level performance of patient recruitment vendors and digital outreach agencies where needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;The Necessities\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;At Entrada, our passion for science, our devotion to patients and our values drives our\u0026amp;nbsp;behavior:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Humanity\u0026lt;/strong\u0026gt; - We genuinely care about patients and about one another.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Tenacity\u0026lt;/strong\u0026gt; - We are relentless and persistent in the pursuit of developing therapies\u0026amp;nbsp;for patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Creativity\u0026lt;/strong\u0026gt; - We are creative problem solvers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Collaboration\u0026lt;/strong\u0026gt; - We are more than the sum of our parts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Curiosity\u0026lt;/strong\u0026gt; - We have a growth mindset and push conventional thought and theory.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;To thrive on our team, you will need to come with:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in life sciences, business, or a related field; advanced degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of progressive leadership experience in clinical operations or related areas, with at least 6 + years focusing on study recruitment, study diversity, and patient engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with rare disease patient populations across global regions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience implementing and executing challenging patient recruitment and retention strategies for late-phase studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Forward-thinking and creative with high ethical standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a fast-paced professional environment with changing priorities and business needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong problem-solving, multitasking, and organizational skills, with the ability to work independently and stay self-directed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This is a US based remote position with preference given to local New England based candidates. This role will require minimum monthly or quarterly travel to the Entrada Therapeutics Headquarters located in Boston, MA.\u0026lt;span style=\u0026quot;color: rgb(255, 255, 255);\u0026quot;\u0026gt;#LI-JF1 #LI-Remote\u0026lt;/span\u0026gt;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;h2\u0026gt;Equal Opportunity Employer\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Third Party Staffing Agencies\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Privacy Statement\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Entrada Therapeutics, Inc. (the “\u0026lt;strong\u0026gt;Entrada\u0026lt;/strong\u0026gt;,” “\u0026lt;strong\u0026gt;we,\u0026lt;/strong\u0026gt;” “\u0026lt;strong\u0026gt;us,\u0026lt;/strong\u0026gt;” or “\u0026lt;strong\u0026gt;our\u0026lt;/strong\u0026gt;”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement \u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.entradatx.com/privacy-notice\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;here \u0026lt;/strong\u0026gt;\u0026lt;/a\u0026gt;\u0026lt;/span\u0026gt;to understand how and when your data is being used.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4059274007,"name":"Clinical Operations \u0026 Biometrics","child_ids":[],"parent_id":null}],"offices":[{"id":4026254007,"name":"Boston, MA","location":"Boston, Massachusetts, United States","child_ids":[4027822007],"parent_id":null}]}],"meta":{"total":7}}