Vacatures 1 tot 10 van 35: clinical trial associate in de regio Amstelveen
ads
- Volledige vacature bekijken
- Volledige vacature bekijken
Oxford Global Resources - Leiden
crucial role within the European Quality Control team, working closely with laboratory professionals to ensure the highest standards in clinical trial support and quality management. This position involves providing expert QC- Volledige vacature bekijken
Jurist - Clinical Trial Center
UZ Leuven - Utrecht
Werken in UZ Leuven? Dan kies je niet voor een job, maar voor een loopbaan. We investeren voortdurend in de talenten en loopbanen van onze - Volledige vacature bekijken
Clinical Research Associate II
Panda Int - Amsterdam
Clinical Research Associate II Location Amsterdam, Netherlands Business Sector Biotechnology Contact email Job ref 23592 Published 11 days ago Clinical Research Associate II Are you an experienced- Preview
Thuiswerkvacatures.net - Amsterdam
bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We are passionate about cultivating- Preview
Thuiswerkvacatures.net - Leiden
In our Clinical Operations team and we are looking for an experienced CLINICAL TRIAL ASSOCIATE to join our growing team and work from our office in Leiden. At Leyden Labs we want to deliver a future- Preview
Associate Scientist - Molecular Microbiology
Oxfordcorp - Leiden
addition, manufacturing processes are optimized and established, and the resulting clinical trial material is evaluated in human clinical studies. We are currently looking for an Assistant Scientist to join the Bacterial Vaccines- Preview
Oxfordcorp - Leiden
clinical trial material; Take part in improvements and innovative projects; Perform data management, acute problem solving, and many other small and diverse tasks; Work on making the processes more efficient for- Preview
Regulatory Affairs Specialist - Dossier Development
Oxfordcorp - Leiden
responsible for all issues regarding CMC. Responsibilities Coordinate and provide technical oversight for the generation of the CMC dossier of marketing and clinical trial submission. Develop the technical eCTD sections