CRA South Germany – Regional Monitoring

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 CRA / Clinical Research Associate Regional Monitoring in South Germany

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 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in Germany

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

If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on 0044 (0) 207 421 0000 or email info@life-science.co.uk

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