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.
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- Country Approval Specialist - FSP dedicated - EMEAThermo Fisher Scientific - Netherlands; Germany; Belgium; France; United Kingdom4 days old
- Information Governance Enterprise Program DirectorMSD - Prague, Czechia; Boxmeer, Netherlands; Rahway, United States4 days old
- Associate Director, Business Development, Digital Technologies – IQVIA Laboratories, Remote Position, Europe.IQVIA - 7 Locations4 days old
- Associate Director - Evidence GenerationGenmab - Utrecht, Netherlands; Copenhagen, Denmark6 days old
- (Associate) Medical Director - Neurology, Western Europe (Client-Dedicated)Thermo Fisher Scientific - Brussels, Belgium; Barcelona, Spain; Milan, Italy9 days old
- Associate Director, Business Development (Central Labs)Thermo Fisher Scientific - Netherlands; Switzerland; Belgium; United Kingdom; Sweden; Denmark; Finland11 days old
- (Senior) Medical Director - Rheumatology (Client - dedicated), EMEAThermo Fisher Scientific - 4 Locations18 days old