We're Hiring: Senior Clinical Data Manager (Contract)
Location: Remote
Travel: Occasional travel to Barcelona, Spain (couple of days per month)
Contract Duration: 6 Months
Industry: Pharmaceutical / Clinical Research
We are seeking an experienced Senior Clinical Data Manager (SCDM) to join a leading integral clinical development environment on an initial 6-month contract. This is an excellent opportunity for a seasoned clinical data professional to play a key role in the oversight and governance of clinical trial data management activities across multiple studies.
Key Responsibilities
- Provide study-level oversight of outsourced Clinical Data Management activities across the full study lifecycle (start-up, conduct, database lock, and close-out)
- Act as the primary Data Management representative within cross-functional study teams
- Review and approve key data management deliverables, including DMPs, DRPs, eCRF specifications, edit checks, and validation documentation
- Oversee CRO/FSP performance, ensuring quality, compliance, and timely delivery of agreed milestones
- Lead data review activities and support database lock readiness
- Monitor data quality, reconciliation activities, and issue resolution processes
- Ensure inspection-ready documentation and compliance with ICH-GCP, GCDMP, and applicable regulatory requirements
Required Experience
- 8+ years of Clinical Data Management experience within a Pharmaceutical, Biotechnology, or CRO environment
- Proven experience leading study-level data management activities across Phase I–III clinical trials
- Strong vendor/CRO oversight experience
- Hands-on involvement in data review, database lock, and submission-ready data delivery
- Experience working in cross-functional global study teams
- Knowledge of CDISC standards and clinical trial data processes
- Experience with EDC platforms (Veeva EDC experience highly desirable)
What We're Looking For
- Strong stakeholder management and communication skills
- Ability to