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Manager, clinical data manager (paradela)

Paradela (Provincia de Ourense)
SRG
Publicada el 7 junio
Descripción

We're Hiring: Senior Clinical Data Manager (Contract)Location: RemoteTravel: Occasional travel to Barcelona, Spain (couple of days per month)Contract Duration: 6 MonthsIndustry: Pharmaceutical / Clinical ResearchWe 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 ResponsibilitiesProvide 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 teamsReview and approve key data management deliverables, including DMPs, DRPs, eCRF specifications, edit checks, and validation documentationOversee CRO/FSP performance, ensuring quality, compliance, and timely delivery of agreed milestonesLead data review activities and support database lock readinessMonitor data quality, reconciliation activities, and issue resolution processesEnsure inspection-ready documentation and compliance with ICH-GCP, GCDMP, and applicable regulatory requirementsRequired 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 integral study teams~ Knowledge of CDISC standards and clinical trial data processes~ Experience with EDC platforms (Veeva EDC experience highly desirable)What We're Looking ForStrong stakeholder management and communication skillsAbility to work independently and manage multiple prioritiesDetail-oriented mindset with a strong focus on data quality and complianceExperience supporting audit and inspection readiness activitiesAdditional InformationRemote 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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