0 - 5 years
7 - 10 Lacs
Posted:5 hours ago|
Platform:
Work from Office
Full Time
q Act as a Study Physician/Co-investigator
q Prepare and review protocols for clinical studies
q Co-ordinate activities related to IEC
q Communicate IEC related issues to all concerned
q Ensure compliance to protocol, SOPs and Regulatory requirements
q Monitor and co-ordinate for volunteer recruitment and screening procedures
q Handle medical confidential reports and case management.
q Coordinate with Project Coordinators for all project related matters
q Monitor and manage adverse events
q Coordinate with panel of consultants to seek medical opinion as and when required
q Ensure timely response to QA findings
q Interact with sponsors on medical related matters
q Handle safety related issues and ensure appropriate communication
q Prepare and review reports for clinical studies
q Write and review related SOPs
q Contribute towards scientific development of the organization
q Help maintain and update all the systems and SOPs in the department
q Train the staff on CPR, GCP and related guidelines and all departmental and relevant SOPs.
Any other responsibilities as assigned by the HOD/Management
Brillex Clinical Research Pvt. Ltd.
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