Shaila Govind

Clinical research and pharmacovigilance professional with 6+ years of experience across clinical trials, medical coding, and pharmaceutical quality systems. Proven expertise in GCP-compliant clinical trial coordination, CRF/EDC management, and medical coding (MedDRA, WHO-DD). Experienced in handling Phase III & IV trials, regulatory documentation, and cross-functional coordination.

Seeking opportunities in Clinical Research, Pharmacovigilance, or Clinical Data Management within Mumbai/Navi Mumbai's CRO, hospital, or life sciences organizations.

Junior Data Analyst (Medical Coding / PV Support) - Cognizant - Airoli (Navi Mumbai)

(2020-06 - 2021-10)

• Performed medical coding using MedDRA & WHO-DD
• Supported Pharmacovigilance team with coding and safety data processing
• Managed uncoded term imports, coded data exports, and dictionary updates
• Raised and prioritized New Term Requests (NTRs)
• Provided coding training and support to PV teams

Associate QC Chemist - Cox Research Centre Pvt. Ltd. - Nashik

(2016-06 - 2017-01)

• Conducted stability testing and quality analysis for pharmaceutical products
• Prepared Certificates of Analysis (CoA) and analytical reports
• Developed and reviewed SOPs and analytical specifications
• Ensured compliance with pharmacopoeial standards and QA protocols

M.Pharm - Pharmaceutics - MVP's College of Pharmacy

PG Diploma in Clinical Research - Clinical Research - ClinTrials Institute

B.Pharm - Pharmacy - MVP's College of Pharmacy