Supriya Chawkekar
Healthcare
About Supriya Chawkekar:
Experienced clinical research and regulatory affairs professional with a strong background in managing clinical trials, regulatory submissions, and pharmacovigilance. Seeking a challenging role to leverage my expertise in ensuring compliance and supporting the successful execution of clinical studies.
Experience
- Assisted in Health Authority submissions for Phase II & III studies in India.
- Coordinated site activities for initial Ethics Committee approvals.
- Managed and updated country and site-level documents to ensure site readiness.
- Created vendors and processed purchase orders in SAP systems.
- Communicated with local authorities on clinical trial activities.
- Managed clinical trial payments, invoices, and fund processing.
- Assisted in site feasibility and site selection during country start-up
- Coordinated with site and internal stake holder for vendor creation, fund (budget) allocation as per SOP or contract within system
- Vendor and payment set up within and for outsource system
- Assisted in agreement finalization and dispatch to site for clinical studies
Education
MSc in Microbiology (2013-2015)
Post Graduate Diploma in Clinical Research
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Assistant Professor, BoS Member, IQAC Coordinator
Education / Training
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