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Job Description & How to Apply Below
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
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 or email Tagged as: cra jobs
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Position Requirements
10+ Years
work experience
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