1 - 4 years
8 - 12 Lacs
Posted:10 hours ago|
Platform:
Work from Office
Full Time
1. Act as a Principal Investigator / Co-investigator in phase-1 studies, Biosimilar and BA/BE studies in all therapeutic area as well as various kind of formulation.
2. Feasibility assessment of different molecules as per request from sponsors.
3. Conducted complex BA/BE study at hospital site as Principal Investigator.
4. Involved in Audit/Inspection handling and Projects conducted as Principal Investigator have been audited and cleared by different regulatory.
5. Leading and guiding the Research Staff as Team Lead.
6. Prepare and review protocols for clinical studies
7. Ensure compliance to protocol, SOPs and Regulatory requirements
8. Communicate IEC related issues to all concerned
9. Coordinate with Project Coordinators for all project related matters
10. Monitor and manage adverse events
11. Coordinate with panel of consultants to seek medical opinion as and when required
12. Ensure timely response to QA findings
13. Interact with sponsors on medical related matters
14. Handle safety related issues and ensure appropriate communication
15. Prepare and review reports for clinical studies
16. Overall supervision of screening and check-in activities
17. Write and review related SOPs
18. Contribute towards scientific development of the organization
19. Support clinical trial group
20. Handle medical confidential report and case management
21. Help maintain and update all the systems and SOPs in the department
22. Train the staff on CPR, GCP and related guidelines and all departmental and relevant SOPs.
23. Any other responsibilities as assigned by the Head of the Department
Lambda Therapeutic Research
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