Vacatures 31 tot 40 van 82
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Freelance Medical Writer Life Sciences)
Yacht - Sassenheim
the Medical Writer may include, but are not limited to, the following: Works independently to write and edit clinical study reports, Investigator’s Brochures, Clinical Trial Results postings, annual reports, and other clinical - Volledige vacature bekijken
Freelance Medical Writer Life Sciences)
Yacht - Weteringbrug
the Medical Writer may include, but are not limited to, the following: Works independently to write and edit clinical study reports, Investigator’s Brochures, Clinical Trial Results postings, annual reports, and other clinical - Volledige vacature bekijken
Freelance Medical Writer Life Sciences)
Yacht - Zoeterwoude
the Medical Writer may include, but are not limited to, the following: Works independently to write and edit clinical study reports, Investigator’s Brochures, Clinical Trial Results postings, annual reports, and other clinical - Volledige vacature bekijken
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
Oxford Global Resources - 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 - Opslaan
Disease mechanisms and new therapies background info...
Radboudumc - Rha
organoids) Clinical trial facilities including outcome measures and support Develop methods to investigate the implementation of person-centered therapies. These include statistics in small groups or n=1 trials as well as- Opslaan
Associate Director Dossier Development
CLS Services via Monsterboard - Leiden
technical eCTD sections to support Regulatory CMC dossier applications. Your responsibilities are: Co-ordinate and provide technical oversight for the generation of the CMC dossier of marketing and clinical trial submissions- 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
Novartis
belang dat we niet alleen naar de vergoeding van één middel kijken, maar het grotere plaatje blijven zien.” Meer weten over wat het werk van Ronald zo waardevol maakt? Nine van Zadelhoff Clinical Study Manager “Ik60+ dagen geleden - Preview - Opslaan
Lead CRA , Oxford Global Resources
Oxford Global Resources
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
Contract Manager bij Clinical Trial Service
Nine Orange - Losser
video die we van deze baan hebben laten maken en kom alles te weten! Clinical Trial Service Kom alles te weten over ons bedrijf Wij zijn een Contract Research Organisatie (CRO) die al 30 jaar gespecialiseerd is in- Preview - Opslaan
Regulatory Affairs Specialist - Dossier Development
Oxford Global Resources - 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- Opslaan
Assistant Scientist - Bacterial Strain Development
Oxford Global Resources - Leiden
immunogenicity and/or efficacy. In 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- Opslaan