Senior Clinical Data Manager

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 global 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 work independently and manage multiple priorities
• Detail-oriented mindset with a strong focus on data quality and compliance
• Experience supporting audit and inspection readiness activities

Additional Information

• Remote contract with occasional travel to Barcelona, Spain for team collaboration and key project activities (typically a few days each month).
• If you’re an experienced Clinical Data Management professional looking for your next contract opportunity, we’d love to hear from you.

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