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Das Unternehmen

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

Rollenbeschreibung

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

Verantwortlichkeiten

- 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

Voraussetzungen

- 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
Veröffentlicht von: SIRE Life Sciences®
Veröffentlicht am: 20-07-2017
Land: The Netherlands
Region: Zuid-Holland
Beschäftigung: Festanstellung
Sachverstand: 3 - 5 Jahre
Standorttyp: Mehrere Standorte
Sprache: Englisch
Sektor: Klinische Forschung
Spezialisierung: Klinik

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Life Sciences

The Netherlands

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