At a Glance
- Tasks: Lead clinical data management for high-stakes trials and mentor junior team members.
- Company: Join a leading biopharma company dedicated to innovation and excellence.
- Benefits: Competitive salary, onsite work, and opportunities for professional growth.
- Other info: Dynamic work environment with potential for hybrid work arrangements.
- Why this job: Shape the future of clinical trials and make a real impact in healthcare.
- Qualifications: 7+ years in biopharma, strong data management skills, and excellent communication.
The predicted salary is between 60000 - 80000 £ per year.
Associate Director of Clinical Data Management – Uxbridge Site
Associate Director of Clinical Data Management to join our Uxbridge site.
This role involves driving clinical trials by owning end‑to‑end data management, setting data standards, leading data quality reviews, mentoring junior leads, and representing data management on cross‑functional and regulatory submission teams.
Responsibilities
- Owning end‑to‑end data management across one or more complex, high‑stakes clinical development programmes – with the autonomy to shape how they run.
- Setting programme‑level data standards in partnership with global teams.
- Leading Data Quality Review meetings, ensuring the integrity and completeness of trial data that underpins regulatory submissions worldwide.
- Mentoring junior Data Management Leads to grow the next generation of talent.
- Representing Data Management on cross‑functional and regulatory submission teams, giving visibility and influence across the full breadth of the organisation.
Qualifications
- 7+ years of experience in biopharma or CRO environments, with at least 3 years in a study or programme leadership role.
- Strong working knowledge of FDA/ICH guidelines and industry data management practices.
- Hands‑on experience with EDC systems, ideally Medidata RAVE.
- A sharp eye for metrics, reporting, and quality oversight.
- Excellent communication skills to hold a room – whether with a junior team member or a senior regulatory authority.
- Bachelor’s degree in life sciences, data science, or statistics (advanced degree a bonus).
Travel: 5–10% to industry conferences, investigator meetings, and regulatory inspections.
Work Environment: Site‑essential roles require 100% onsite shifts. Site‑by‑design roles may be eligible for a hybrid work model with at least 50% onsite.
Equal Employment Opportunity
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Applicants can request a reasonable workplace accommodation or adjustment prior to accepting a job offer.
If you require reasonable accommodations or adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms. com.
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