Clinical Research Associate (Level I) - Netherlands, client dedicated
Core
Conducts remote or on-site clinical monitoring and site management to ensure protocol and regulatory compliance, guaranteeing subject rights and data reliability for pharmaceutical and biotech clients.
Role type
Level I Clinical Research Associate (CRA)
Builds
Clinical trials across 100+ countries for top 50 pharmaceutical companies and 750+ biotech firms
Domain
Life Sciences / Clinical Research / Pharmaceutical
Required skills
Clinical monitoring, ICH-GCP guidelines, Risk Based Monitoring, Root Cause Analysis, Data review (SDR/SDV/CRF), Investigational product inventory, Site initiation, Trial close out, Regulatory compliance
Preferred skills
Medical/therapeutic area knowledge, Critical thinking, Problem solving, Microsoft Office
Technologies
Clinical Trial Management System (CTMS)
Responsibilities
Monitor investigator sites using risk-based approach; Conduct on-site and remote monitoring visits; Ensure data accuracy through document review; Initiate and close out clinical trial sites; Participate in investigator meetings; Respond to audits and inspections; Maintain essential study documents.
Seniority
Junior, entry-level IC