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The company

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

Role description

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

Responsibilities

- 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

Requirements

- 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

Life Sciences

The Netherlands

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 20 658 9800

Belgium

Science 14 Atrium
14b, Rue de la Science
1040 Bruxelles
+32 (0) 2 588 1277

Germany

Fünf Höfe
Theatinerstraße 11
80333 München
+49 (0) 89 3803 8966

The Netherlands

ROOOMS Maastricht
Boschstraat 21
6211 AS Maastricht

Information Technology

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Calypso Building
Kruisplein 480
3012 CC Rotterdam
+31 (0)10 316 1066

Chemicals

The Netherlands

Groot Handelsgebouw
Stationsplein 45 4th Floor
3013 AK Rotterdam
+31 (0)85 044 4610

Healthcare

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