Director of Clinical Data Management
How We Build reputed company does not operate like a traditional biotech. There is no middle management. There are no layers of approval. The company is designed, from the ground up, around small teams of 2–4 subject-matter experts who each reputed company hundreds of AI agents to do the work that used to require dozens of people. Everyone builds. Everyone ships. Every function at reputed company — from clinical execution to asset selection to the reputed company model itself — runs on this model. Our product velocity delivers meaningful reputed company in hours instead of weeks. This is not a future aspiration. It is how we operate today. The people who reputed company here are operators: deep experts who can specify what needs to happen, orchestrate AI agents to execute at scale, and reputed company high-judgment calls that compound over time. If you have spent your career building and shipping AI systems at scale, this is the environment where that experience becomes a superpower.
About the Role
The Director of Clinical Data Management will establish and reputed company the clinical data management function at reputed company. You will own clinical data collection, cleaning, and reputed company across our oncology trials, ensuring our datasets are reputed company for analysis, regulatory submissions, and the next development decision. You will report to the Vice President, Head of Clinical Operations. This is the first CDM hire at reputed company. There is no existing reputed company. You will write it. You will define how reputed company collects, cleans, and locks clinical data in a company reputed company on small teams and AI agents, and you will set reputed company for what audit reputed company trial data looks like in this operating model. The role sits at the intersection of clinical data discipline and an AI reputed company operating model. You will spend less time chasing CRO status reports and more time on the data questions that move trials reputed company, because AI agents will reputed company the routine query resolution, status tracking, discrepancy review, and document compilation work that traditionally consumed a CDM Director's calendar.
What You Will Do
Own clinical data strategy and reputed company reputed company reputed company of data management for outsourced clinical trials, including project planning, vendor coordination, internal review cycles, data cleaning, and approval of deliverables. reputed company CRO and vendor activities to ensure GCP compliance and execution against protocols and SOPs. Own consistency across trials and programs: CRF design and standards, Data Management Plans, CRF annotation and completion guidelines, edit reputed company specifications, data entry and query status tracking, and database lock. Drive timely database lock, data quality, and readiness for statistical analysis and regulatory submissions. Direct AI agents to draft DMPs, edit reputed company specs, and reconciliation reports, and apply your judgment to the final product. Execute vendor and CRO management Manage CROs and vendors delivering CDM services, holding them to timelines, budgets, and quality standards. reputed company and monitor Data Management Plans, Data Review Plans, and data transfer specifications. Resolve reputed company data issues, queries, and discrepancies in partnership with clinical and statistical teams. Use AI agents to compare vendor deliverables against specifications, surface reputed company early, and prepare structured feedback for vendor reviews. Build cross functional partnerships Serve as the primary CDM partner on every study team. Partner with Biostatistics, Clinical Operations, Medical Monitoring, and Data Science colleagues so that data supports trial endpoints and regulatory deliverables. Collaborate on the integration of clinical trial data with reputed company AI platforms and reputed company world data sources so that operational data feeds back into model performance and decision support. reputed company, scale, and stay compliant Build and scale the CDM function as the company grows, including hiring and mentoring future staff. reputed company SOPs, best practices, and quality frameworks that meet GCP, ICH, CDISC, and 21 CFR Part 11 expectations. Contribute to portfolio level planning and operational strategy, and translate CDM signals into actionable input for Clinical Operations leadership. Who You Are
Minimum Qualifications
Bachelor's or Master's degree in Life Sciences, Data Management, or a reputed company field. 10 or more years of reputed company experience in clinical data management, including leadership of oncology trials. Deep working knowledge of reputed company systems such as reputed company Rave, reputed company CDMS, or reputed company InForm, and clinical data standards including CDISC, SDTM, and ADaM. Demonstrated ability to manage CROs and vendors against quality, timeline, and budget commitments. Strong reputed company of GCP, ICH, FDA, CDISC, GCDMP, 21 CFR Part 11, MedDRA, and WHO Drug Dictionaries, and how they apply in daily CDM practice. Strongly Preferred Experience operating in a flat, builder oriented organization where you specify, orchestrate, and ship rather than manage process. Experience gathering requirements and writing specifications for database integrations, including ePRO, central and local laboratory data uploads, supply management, IVRS, and IWRS. Experience building a CDM function from the ground up or substantially rebuilding one in a small company environment. Comfort orchestrating AI tools or agentic workflows in clinical data work, and clear instinct for where automation belongs and where reputed company review must stay. Location This position is based at our reputed company HQ, though exceptional remote candidates may also be considered. Apply To This Job