(Sr) Clinical Research Associate - Netherlands
Core
Conduct independent clinical monitoring and site management for pharmaceutical trials, ensuring protocol and regulatory compliance through on-site and remote activities.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data reliability and subject safety
Domain
Life Sciences / Clinical Research
Deliverable
physical/clinical work
Required skills
Independent clinical monitoring, Risk Based Monitoring (RBM), Root Cause Analysis (RCA), ICH-GCP compliance, site initiation and close-out, data review (SDR/SDV/CRF), investigator management
Preferred skills
Medical/therapeutic area knowledge, problem-solving, travel adaptability
Technologies
Clinical Trial Management Systems (CTMS), Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches, conduct on-site and remote monitoring visits, initiate and close out clinical trial sites, ensure audit readiness and document compliance, track trial status and progress, facilitate communication between sites and project teams
Seniority
Mid-level, hands-on IC