Associate Director - Data Management

As Associate Director of Data Management, you will provide strategic leadership and operational oversight for all data management activities across multiple global clinical programmes. You'll oversee CRO partners, implement data governance frameworks, and ensure the timely delivery of compliant, submission-ready data. This role spans end-to-end ownership, from database design and study start-up to database lock and regulatory submission, and offers the chance to influence technology strategy and inspection readiness at scale., * Lead data management strategy across global studies, ensuring compliance, efficiency, and regulatory alignment.

• Manage full study lifecycle: DMP development, edit check design, database testing, data cleaning, and lock.
• Serve as the subject matter expert for Medidata Rave, RTSM, eCOA, Coder, and related systems.

You'll excel in this role if you bring:

• 10+ years of experience in Clinical Data Management.
• Proven expertise with Medidata technologies (Rave, RTSM, eCOA, Coder) and integrated data platforms.
• Experience supporting global regulatory submissions (NDA, BLA, MAA) and inspection readiness.

This forward-thinking biopharma company is advancing its digital R&D ecosystem to accelerate clinical and regulatory innovation through connected, compliant, and data-driven technologies. Operating across global therapeutic programmes, the organisation combines science, technology, and quality to drive efficient, inspection-ready development. As part of the Global Biometrics function, you'll play a key role in building the company's next-generation data management capability, defining standards, systems, and partnerships that ensure data integrity, quality, and traceability across all trials.