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Senior clinical data manager (paradela)

Paradela (Provincia de Ourense)
SRG
Publicada el 6 junio
Descripción

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 general 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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