Clinical Research Associate (CRA) jobs in The Netherlands
Clinical Research Associates (CRAs) are professionals who play a crucial role in the field of clinical research. Their primary responsibility is to monitor and oversee clinical trial activities to ensure the safety, efficacy, and compliance of new drugs or medical devices. CRAs work closely with investigators, healthcare providers, and study participants to ensure that all protocols, procedures, and regulations are followed. They review study documents, collect and analyze data, and ensure the accuracy and integrity of clinical trial data. Additionally, CRAs may also assist in the preparation and submission of regulatory documents to the relevant authorities. Overall, this profession requires strong attention to detail, excellent organizational and communication skills, and a comprehensive understanding of ethical and regulatory guidelines in clinical research.
Found jobs - 63
Exact matches
Senior Clinical Research Associate (Site Manager)Johnson & Johnson - Breda, Netherlands; Beerse, BelgiumPosted 30+ days ago
Related matches
Senior Business Application Engineer – Research Digital SystemsGenmab - Utrecht, Netherlands4 days old
Senior Project Specialist (Sponsor Dedicated) The NetherlandsSyneos - Amsterdam, Netherlands5 days old
Associate Director, Evidence GenerationGenmab - Utrecht, Netherlands; Copenhagen, Denmark; Princeton, United States5 days old
Intern, Quality & Compliance (Data, Digital & AI Department)Genmab - Utrecht, Netherlands11 days old
Regulatory Affairs Manager - Market AccessThermo Fisher Scientific - Basingstoke, United Kingdom12 days old
Vice President, Global Total RewardsGenmab - Utrecht, Netherlands; Copenhagen, Denmark; Princeton, United States16 days old
Intern, Translational & Quantitative Data Science (Streamlining Biomarker Operations: Transforming Clinical Inventory Management with Automation and AI)Genmab - Utrecht, Netherlands17 days old
Intern, Translational Data Science (Project: Computational and Molecular Approaches to Improve Preclinical Risk Assessment of Biologics)Genmab - Utrecht, Netherlands17 days old
Principal Medical Writer - Regulatory Submission DocumentsSyneos - Amsterdam, Netherlands17 days old
Principal Medical Writer - Submission Docs (2.5/2.7.2/2.7.3/2.7.4) - Oncology - Remote BasedSyneos - Amsterdam, Netherlands17 days old
Senior Analyst Technical Product Management - A2RJohnson & Johnson - Breda, Netherlands; Prague, Czechia; Beerse, Belgium19 days old
Associate Director, Global Trial LeadGenmab - Utrecht, Netherlands; Copenhagen, Denmark; Princeton, United States26 days old
Principal Biostatistician (Medical Affairs/HEOR - Europe Only)Syneos - Amsterdam, NetherlandsPosted 30+ days ago
Senior Principal Medical Writer - Regulatory - Oncology - Single SponsorSyneos - Amsterdam, NetherlandsPosted 30+ days ago
Director, Tech Lead - Data PlatformGenmab - Utrecht, Netherlands; Copenhagen, Denmark; Princeton, United StatesPosted 30+ days ago
(Associate) Medical Director - Rheumatology, EMEAThermo Fisher Scientific - Brussels, Belgium; Milan, ItalyPosted 30+ days ago
Director, Development Sourcing and Vendor ManagementGenmab - Utrecht, NetherlandsPosted 30+ days ago
Vice President, Head of Global Translational Medicine & ResearchGenmab - Utrecht, Netherlands; Princeton, United StatesPosted 30+ days ago
Dermatologist - Medical DirectorMedpace - Madrid, Spain; Maastricht, Netherlands; Stirling, United KingdomPosted 30+ days ago



