Vacatures 41 tot 50 van 75
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Senior Pharmaceutical Operator
Checkmark Labrecruitment - Leiden
In this role as Senior Pharmaceutical Operator you will take part on all activities related to the cGMP production of Clinical Trial Material (CTM)- Volledige vacature bekijken
Clinical Trial Manager - - Infectious Disease
MEDPACE - Maastricht
Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to- Volledige vacature bekijken
Clinical Trial Manager - - Infectious Disease
MEDPACE - Rotterdam
Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to- Volledige vacature bekijken
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
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
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
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
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
Oxfordcorp
assigned projects with minimal supervision. S/he ensures clinical trial data collected meet the highest standards of data integrity, while meeting timelines and budgets. Responsibilities Reporting to the Manager , Data60+ dagen geleden - Preview - Opslaan
Oxfordcorp
Description The Clinical Research Associate (CRA) will support regional conduct of clinical research within clinical research centers that are actively participating in clinical trials. The CRA will act as the site manager for60+ dagen geleden - Preview - Opslaan
Oxfordcorp
Protocol Deviations (minor/major) Communication with all involved parties (EDC, STAT, MA, Clinical teams, Client, External Data Providers, Medical Writing, Project Manager Biometrics) … Processing of (Interim) Database60+ dagen geleden - Preview - Opslaan
Junior Clinical Research Associate (Junior CRA)
Oxfordcorp
Responsibilities: Evaluate, initiate, monitor & close out clinical trial sites. Ensure site compliance and data quality Respond to site-related queries and escalates issues Responsible for operational site management60+ dagen geleden - Preview - Opslaan