Associate Director, Clinical Data Management

Associate Director, Clinical Data Management Cambridge, MA Company Overview Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology & oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. Position Overview Prime Medicine is seeking an experienced Associate Director of Clinical Data Management to lead clinical data strategy and execution across gene editing programs from first‑in‑human studies through regulatory submission. This role will oversee all internal and external data management activities supporting INDs, CTAs, BLAs, and global regulatory filings. The ideal candidate has experience in rare disease clinical trials, vendor oversight, and complex biologic or gene therapy programs, and is comfortable operating in a fast‑paced environment. This individual will ensure clinical data integrity, regulatory readiness, and high‑quality execution across the development portfolio. This role reports to the Senior Director, Clinical Operations. Key Responsibilities Clinical Data Leadership Lead all clinical data management activities across multiple programs from IND through BLA submission. Develop and execute data management strategies aligned with regulatory requirements both in the US/ex‑US. Oversee CRF design, database build, edit checks, data review, coding, reconciliation, and database lock. Ensure implementation of CDISC standards (SDTM/ADaM) to support submission readiness. Support inspection readiness and maintain audit‑ready documentation. Lead selection, oversight, and performance management of CRO and data management vendors. Manage vendor budgets, timelines, KPIs, and quality metrics. Oversee external data transfers and reconciliation processes (e.g., SAE, lab, PK and PD). Ensure change control, database archiving, and data governance processes are compliant and well documented. Gene Therapy & Rare Disease Expertise Oversee integration of complex data streams including: Genomic and sequencing data Biomarker and translational endpoints Immunogenicity and PK/PD Long‑term follow‑up safety data Support dose‑escalation studies with rapid data review cycles and SRC/DMC readiness Tailor data processes to rare disease trial realities (small populations, adaptive designs, multi‑cohort studies). Systems & Infrastructure Contribute to scalable data infrastructure and identification of key efficiencies between programs. Support implementation and optimization of EDC, ePRO, IRT, and data visualization systems. Ensure integration between clinical data, laboratory systems, and sample tracking systems. Cross‑Functional Collaboration Partner with Clinical Development, Clinical Operations, Regulatory, Quality, and Translational Sciences. Serve as subject matter expert for data standards, governance, and process improvement initiatives. Contribute to development and improvement of internal SOPs and workflows. Qualifications Bachelor’s degree in life sciences, statistics, informatics, or related field (advanced degree preferred). 8+ years of progressive clinical data management experience, including leadership responsibility. Experience supporting IND submissions and major regulatory filings (BLA/NDA/MAA). Direct experience in rare disease and/or gene therapy, gene editing, or advanced biologics strongly preferred. Demonstrated CRO/vendor oversight experience in global trials. Strong knowledge of ICH/GCP, FDA/CFR regulations, CDISC standards, and eCTD submission requirements. Experience with EDC systems, medical coding (MedDRA/WHO Drug), and external data integration. Strong understanding of safety data reconciliation and regulatory inspection preparedness. Excellent organizational, project management, and communication skills. Strategic thinker with strong execution skills. Detail‑oriented with high standards for data quality and compliance. Collaborative and cross‑functional mindset. Comfortable working in a dynamic, innovative biotech environment. Passion for advancing transformative therapies for patients with rare genetic diseases. The pay range reflects the full‑time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short‑term incentive award (e.g., bonus) and an annual long‑term incentive award (e.g., equity). Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company‑wide recharge breaks. U.S. Pay Range $174,000 - $212,000 USD Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law. #J-18808-Ljbffr