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Senior Medical Writer remote Life Sciences

Yacht - Utrecht
responsibilities of the Principal 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
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Internship Regulatory Affairs

Randstad - Leiden
regulations related to Clinical Trial Applications and the internal Johnson & Johnson procedures on managing initial CTAs and submission activities to maintain the regulatory approval for different clinical trials. In addition, during
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Administrative Assistant - Relocation to The

Work in holland (Workinholland) - Utrecht
Looking to start a new career in The Netherlands? LabourLink is seeking a dedicated Administrative Assistant to join an energetic and growing team. If you have strong communication skills and enjoy managing office tasks in a
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Administrative Assistant

Oxfordcorp
varied job within the context of clinical trials. Function Description The administrative assistant provides support in a wide range of tasks related to the clinical trials run by our pharma client. Responsibilities
60+ dagen geleden - Preview

Experienced CTA / Study Start-up Support Specialist

Oxfordcorp - Noord-Brabant
Are you an experienced Clinical Trial Assistant / Study Start-up Support Specialist? You work independently and are fluent in English & in French? Have you ever been responsible for the administrative support and
60+ dagen geleden - Preview

Clinical Project Manager

Oxfordcorp
budget reports distribution to the sites Oversee the Clinical Research Associates (CRAs) spread over Europe for all activities related to monitoring of the Clinical trial locally. Oversee the Clinical Trial Assistant (CTAs
60+ dagen geleden - Preview

Associate Scientist - Molecular Microbiology

Oxfordcorp - Leiden
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 join the Bacterial Vaccines
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Jr Clinical Trial Assistant

Oxfordcorp
Ben jij een administratieve duizendpoot en wil je de dynamische wereld van klinische studies leren kennen? Dan hebben wij dé baan voor jou! Sluit je aan bij ons internationale team en wees de belangrijke sleutel in de onders
60+ dagen geleden - Preview

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

Study Start Up Associate I - Dutch Speaker

Icon Plc - Utrecht
What You Will Be Doing: Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions. Coordinating with internal and external stakeholders to
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Study Start Up Associate I - Dutch Speaker

Icon Plc - Utrecht
submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications. Coordinating and liaising with internal and external stakeholders to obtain necessary
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Clinical Trial Assistant

Icon Plc - Amsterdam
JR119275 Clinical Trial Support ICON Full Service & Corporate Support Office Based Hi, I am Rajkapoor and I manage this role View my profile Email Rajkapoor.Kamaludeen@iconplc.com View my other
FULL_TIME - Preview

IHCRA in (PRA) ICON

Icon Plc - Utrecht
as assigned You will need: Minimum Bachelor's degree in a life science At least 12 months of a CTA/ Clinical Trial Assistant or similar role experience within the clinical /pharmaceutical industry Understanding
FULL_TIME - Preview