Clinical Trials

3 days ago


Hyderabad, India Advity Research Full time

Hyderabad 02 to 06 Years Full Time
- Plan and conduct investigator site selection audits and clinical trial study audits at investigator sites in accordance with applicable GCP guidelines and regulations.
- Review of CRF design
- Review of standard operating procedures
- Issue audit reports to the investigator site staff and other concerned study personnel
- Review and assess the audit responses/CAPA and closure of the audit report in a timely manner.
- Provide regular updates of non-compliance or major findings in clinical trials to the Head-Quality Assurance
- Review of Clinical study report
- Provide document review comments in a timely manner.



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