Vacatures 31 tot 40 van 69
ads
- Volledige vacature bekijken
- Volledige vacature bekijken
- Volledige vacature bekijken
Jurist - Clinical Trial Center
UZ Leuven - Lent
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 - Mechelen
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
PPD B. V. - Bennekom
We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in - Volledige vacature bekijken
Oxfordcorp - Rotterdam
maintenance of study monitoring plan, templates, trackers, study tools, and site-specific documents. Assists Clinical Study Manager (CSM) with development of human clinical protocol, investigational plan/brochure, SIV training- Preview - Opslaan
Country Study Start-up Specialist FR/EN)
Oxfordcorp
agreements. Ensure clinical trial management systems containing all country and site-specific information are maintained and kept current during start up and study maintenance. Manage translations needed for regulatory60+ dagen geleden - Preview - Opslaan
Oxfordcorp
Clinical Trial Agreement (CTA) template per sites, FU on the signature collection and make sure archiving is correctly done. Archiving on Recpoint LMA studies Working across teams to develop and maintain operational60+ dagen geleden - Preview - Opslaan
Opportunities Schmidt Consultancy
Schmidt Consultancy - Zutphen
60% of the cancer patients desire to participate in clinical trials. Only 5% actually does. To bridge this gap our client makes clinical trial protocols direct, online and easy to find, available for oncologist and patients- Opslaan
Regulatory Affairs Administrator
Oxfordcorp
administrative preparation & follow-up of clinical trial applications (CTAs) and relevant documents. You adapt CTA file to country specific and local requirements. You submit, follow-up and tracking of CTAs according to60+ dagen geleden - Preview - Opslaan
Nine Zadelhoff Novartis past heel goed bij mij
Novartis
Nine van Zadelhoff werkt al 15 jaar bij Novartis, ze heeft het dan ook erg naar haar zin als clinical study manager (CSM). Ze werkt op de afdeling Trial Monitoring Operations (TMO), die toezicht houdt op de studies van60+ dagen geleden - Preview - Opslaan
Oxfordcorp - Leiden
trial . Examples of immunological assays that are performed are: ELISA, T cell ELISpot, cytokine staining (intracellular) and virus neutralization assays (VNA). The main responsibility of the Scientist clinical immunology is to- Preview - Opslaan
Clinical Research Associate (CRA) - DU/FR/EN
Oxfordcorp
Responsibilities You evaluate, initiate, monitor & close out clinical trial sites. You ensure site compliance and data quality You respond to site-related queries and escalates issues You responsible for operational site60+ dagen geleden - Preview - Opslaan
Oxfordcorp
For one of our clients in Zaventem, we are currently looking for a " Clinical Data Manager ". Job Description The Senior Clinical Data Manager will be responsible for all aspects of clinical data management associated60+ dagen geleden - Preview - Opslaan