Vacatures 61 tot 70 van 103
ads
- Volledige vacature bekijken
- Volledige vacature bekijken
International Product Manager Look-O-Look
Perfetti van Melle Benelux B.V. - Breda
International Product Manager Look-O-Look Apply now Date: May 30, 2024 Location: Breda, NB, NL, 4815 HK Company: Perfetti Van Melle YOU + US? Ben jij klaar voor een frisse stap in jouw carrière? Wij hebben namelijk ‘a- Volledige vacature bekijken
Ilionx - Zwolle
zowel elkaar als met de klant. Jouw manager zorgt hierin vooral voor een prettige werkomgeving waarin hij jouw persoonlijke ontwikkeling én de samenwerking met jouw collegas juist alleen maar zal aanmoedigen. Als voormalig- Volledige vacature bekijken
Oxford Global Resources
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 regulatory activities60+ dagen geleden - Preview
Oxford Global Resources - 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
Scientist Immunology / Biomarkers
Oxford Global Resources - Leiden
efficacy. In addition, manufacturing processes are optimized and established, and the resulting clinical trial material is evaluated in human clinical studies. The biomarker immuno team supports the vaccine development team in- Preview
Derksenderks via Monster Worldwide - Leiden
cycle reviews. You assure the completeness of the Product Specification File and the Study File to facilitate certification of clinical trial materials by the Qualified Person. As QA Manager you participate and contribute toCountry Study Start-up Specialist FR/EN)
Oxford Global Resources
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
Oxford Global Resources
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
Regulatory Affairs Administrator
Oxford Global Resources
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
Oxford Global Resources - 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
Clinical Research Associate (CRA) - DU/FR/EN
Oxford Global Resources
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
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