Senior Clinical Research Associate (Netherlands)
Core
Oversees clinical monitoring and site management to ensure protocol adherence, data accuracy, and regulatory compliance for clinical trials.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical trial data and site compliance
Domain
Clinical Research / Life Sciences
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical monitoring, site management, protocol adherence, GCP/ICH-GCP compliance, source data verification, CRF review, safety event documentation, protocol deviation management, corrective and preventative actions, data query resolution, site feasibility evaluation, training and mentoring, stakeholder engagement, medical terminology knowledge
Preferred skills
Experience with complex studies, process improvement, SOP development, travel readiness
Technologies
MS Office, EDC systems
Responsibilities
Conduct on-site and remote monitoring visits (SIVs, routine, close-out); verify source data and CRFs for accuracy; review safety events and protocol deviations; manage data queries and action items; lead site feasibility activities; train and mentor site staff and CRAs; support investigator meetings and internal/external communications.
Seniority
Senior, hands-on IC with mentorship responsibilities
