Klinischer Monitor / Clinical Research Associate / CRA (m/w/d) Home Office based
Offer summary
Qualifications:
Bachelor's degree in life sciences or related field., Experience in clinical monitoring or clinical research., Strong understanding of GCP and regulatory requirements., Excellent communication and organizational skills..Key responsibilities:
- Monitor clinical trial sites to ensure compliance with protocols.
- Conduct site visits and prepare reports on findings.
- Collaborate with investigators and site staff to facilitate study progress.
- Assist in the training of site personnel on study procedures.
Required profile
Experience
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