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Senior CRA

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L'entreprise

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

Description du rôle

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

Responsabilités

- 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

Exigences

- 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®

Réf. nombre: 34075
Placé par: SIRE Life Sciences®
Posté le: 20-07-2017
Pays: The Netherlands
Région: Zuid-Holland
Emploi: Permanent
Compétence: 3 - 5 années
Type de lieu: Plusieurs emplacements
Langue: Anglais
Secteur: Recherche clinique
Spécialisation: Clinique

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