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Freelance Interim Hoofd CIO-Office (ZZP)

public.client.yacht.display.name - Groningen
Interim Hoofd CIO- Office - Rijksuniversiteit Groningen In verband met langdurige ziekte zijn wij voor het Team CIO- Office van het Centrum voor Informatietechnologie (CIT) op zoek naar een enthousiaste en stimulerende manager
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Clinical Research Regulatory Coordinator

Oxford Global Resources
clinical pharmacology principles, with ability to review emerging safety and efficacy profile of a drug candidate and recognize potential serious adverse effects;Demonstrated understanding of the complexities and recent developments
60+ dagen geleden - Preview

Epidemiologist

Epidemiologie
statisticians, data analysts, medical writers, safety and pharmacovigilance specialists, project managers and office support staff spread over more than 10 countries. Our headquarters are in Leuven, Belgium but all of our staff
60+ dagen geleden - Preview

Epidemiologist

Epidemiologie
medical writers, safety and pharmacovigilance specialists, project managers and office support staff spread over more than 10 countries. Our headquarters are in Leuven, Belgium but all of our staff work remotely. You may
60+ dagen geleden - Preview

Clinical Trial Assistant

Oxford Global Resources
Do you actively want to contribute supporting drug development in one of the biggest biotech companies with an amazing pipeline? Then this is the job for you! Job Description As a Clinical Trial Assistant (NL/EN or FR
60+ dagen geleden - Preview

Project engineer

Oxford Global Resources
description Our client has a long history in Belgium, as it was in Brussels that the group established its first European office in the 1950s. A long tradition of innovation and investment in biomedical research. Today, our 4
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Senior PV Associate

Oxford Global Resources
Case processing experience a plus Knowledge and experience of databases (preferably safety or regulatory or similar environments) Excellent knowledge of Microsoft Office Ability to work under pressure and in a
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Medical Manager Associate

Oxford Global Resources
location is our office in Brussels with the flexibility to work from home. Responsibilities Communicate and exchange medical and scientific information and clinical data Provide therapeutic area and drug expertise to the
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Wil je zoals deze

Criver via Monster Worldwide - Den-bosch
preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total
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Drug Safety Officer / / vaste aanstelling

Pharmamediair.nl - Amersfoort
Farmaceutisch bedrijf omgeving Amersfoort. Aannemen en afhandelen van telefonische en schriftelijke medische vragen/bijwerkingen van afnemers en patiënten. Registreren van deze meldingen in het systeem, verwerken en doorstu
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Drug Safety Officer

Pharmamediair.nl - Amsterdam
Deze vacature staat offline! De opdrachtgever Farmaceutisch bedrijf in Amsterdam. De omschrijving The Drug Safety Officer is responsible for support on pharmacovigilance ( drug safety ) requirements performed on
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