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Het bedrijf

Our client is a professional Clinical Research organization, based in Zuid-Holland Netherlands. The company is a CRO for pharmaceutical, biotechnology and medical devices companies

Functie omschrijving

You will act as a member of the clinical monitoring team with the responsibility that everything is compliant with study guidelines, SOPs etc.

Verantwoordelijkheden

- Perform site visits and monitor activities in accordance with protocol, GCP/ICH Guidelines, and other applicable regulatory requirements.
- Mentor CRAs.
- Evaluate overall performance of site and site staff .
- Maintain working knowledge of GCP/ICH Guidelines

Vereisten

- Bachelor degree in relevant field
- 2+ years of prior clinical monitoring experience
- GCP/ICH knowledge
- Excellent communication skills in Dutch and Englisch



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SIRE Life Sciences®

Ref. nummer: 34075
Geplaatst door: SIRE Life Sciences®
Geplaatst op: 20-07-2017
Land: The Netherlands
Regio: Zuid-Holland
Dienstverband: Permanent
Expertise: 3 - 5 jaar
Locatie Type: Meerdere locaties
Taal: Engels
Sector: Clinical Research
Specialisatie: Clinical

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Contact

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6211 AS Maastricht


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