Vacatures 1 tot 10 van 27
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Principal Medical Writer (remote) Life Sciences)
Yacht - Utrecht
following: Works independently to write and edit clinical study reports, Investigator’s Brochures, Clinical Trial Results postings, annual reports, and other clinical regulatory documents across multiple therapeutic areas as assigned- Volledige vacature bekijken
Jurist - Clinical Trial Center
UZ Leuven - Wons
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
Jurist - Clinical Trial Center
UZ Leuven - Brakel
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 (CRA)
Panda Int - Ede
by excellence and looking for a dynamic career in clinical research, this role is for you. Responsibilities Monitor clinical trial sites: Ensure protocol compliance and regulatory adherence through on-site and remote- Preview - Opslaan
Datamanager Trialbureau Interne Geneeskunde
Nvz-kennisnet - Sittard
systemen zodat de uiteindelijke uitkomsten van de studies betrouwbaar en naar waarheid zijn. Medische kennis en/of achtergrond is hierbij een absolute pré. Verder is een Good Clinical Practice (GCP) certificaat verplicht. Wanneer- Preview - Opslaan
Clinical Research Associate II Parexel
Parexel via Jobsonline - Zwolle
This role can be office-based in Amsterdam or decentralized in the Netherlands. Your time here At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor . CRA’s are- Preview - Opslaan
Internship Integrated Data Analytics and Reporting
VacatureVizier - Leiden
of trial level data management activities per applicable procedures, with direction from the Data Management Leader, Global Data Manager or Clinical Data manager. May include scientific study data review and management of- Opslaan
Senior CRA (sponsor dedicated)
Icon Plc - Utrecht
Permanent Description TMF Specialist is to perform all duties related to the timely processing of essential and non-essential clinical trial documents to facilitate study startup, drug shipment, eTMF maintenance and suppo- Preview - Opslaan
Vacatures, Stoevelaar - Amsterdam
flexibele, bezoeken, assurance, biomedical, brabant, detachering, branche, buitendienst, business, gezondheidszorg, calculator, care, carriere, hbo, v, celbioloog, chemical, chemici, carrière, chemicus, biotech, chemisch, clinical - Opslaan
Corsano - The Hague
forefront of developing, producing, and selling medically certified wearables for continuous vital sign monitoring. Our flagship product, the Corsano Solution, is a CE and FDA certified system designed to monitor heart rate, atrial- Preview - Opslaan
NLF Fortrea Netherlands via Jobsonline - Amsterdam
collecting investigator documentation and site management Provide coverage for clinical contact telephone lines, as required Update, track and maintain study-specific trial management tools/systems Generate and track drug- Preview - Opslaan
Icon Plc - Amsterdam
all duties related to the timely processing of essential and non-essential clinical trial documents to facilitate study startup, drug shipment, eTMF maintenance and suppo - Preview - Opslaan
Lead CRA , Oxford Global Resources
Oxfordcorp
work on the frontline of communication with project stakeholders, ensuring the successful conduct of clinical trials in a variety of therapeutic indications. You will supervise study start-up and site management activities to60+ dagen geleden - Preview - Opslaan