Senior Clinical Monitor - Phase II/III, GCP Expert

Senior Clinical Monitor - Phase II/III, GCP Expert

Vollzeit Kein Homeoffice möglich
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Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a senior CRA Home Based in Germany in one of the major cities to work sponsor dedicated.

Job Overview

  • Monitoring clinical studies in phases II-III
  • Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
  • Identification, qualification and initiation of investigators and their sites.
  • Supervising study conduct according to GCP requirements and all applicable laws.

Key Requirements

  • Bachelor degree in life-science
  • Min 4 year monitoring experience as CRA within a CRO, Pharma, Biotech
  • Experience in commercial studies
  • Experience with site initiation, site close out
  • Experience in clinical studies phase II-III
  • Fluent English & German
  • Excellent communication skills
  • A full clean drivers license
  • FTE: 1.0

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Kontaktdaten:

Resourcing Life Science Recruiting-Team