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Clinical Trial Assistant

Oxford Global Resources
Ben jij een administratieve duizendpoot en wil je de dynamische wereld van klinische studies leren kennen? Dan hebben wij dé baan voor jou!
60+ dagen geleden - Volledige vacature bekijken

Interim/ Consultant Director, Facility Manager

Genmab - Utrecht
At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment a
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Internship Clinical Trial Laws And Regulations

Randstad - Leiden
Do you want to gain valuable experience as an intern in a highly dynamic department of a top pharmaceutical company – Johnson & Johnson?We
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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 to
60+ dagen geleden - Preview - Opslaan

Clinical Research Associate

Icon Plc - Amsterdam
company dedicated to be an innovative, research driven biopharma, with a stable pipeline of innovative products. ICON has a large and dedicated team of Clinical Trial Assistants, Clinical Research Associates, Clinical Trial
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Regulatory Affairs Specialist - Dossier Development

Oxfordcorp - 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
INTERN - Opslaan

Assistant Scientist - Bacterial Strain Development

Oxfordcorp - 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
INTERN - Opslaan

Clinical Contracts Associate (DU/FR/EN)

Oxfordcorp
work from our client's office in Brussels and you will report to the Manager Clinical Contracts EMEA region, based in Germany. You are responsible and accountable for preparation, negotiation and signature of clinical
60+ dagen geleden - Preview - Opslaan

Country Start-up Specialist

Oxfordcorp
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 activities
60+ dagen geleden - Preview - Opslaan

QA Technology Manager

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 to
CONTRACTOR - Opslaan

Scientist Immunology / Biomarkers

Oxfordcorp - 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
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CRA for the EN)

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
FULL_TIME - 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 regulatory
60+ dagen geleden - Preview - Opslaan