Bhakti Gavhane
@bhaktigavhane
I validate clinical documentation, maintain compliance, and coordinate workflows for global trials and laboratory operations.
IndiaWhat I'm looking for
At Tata Consultancy Services, I process and validate clinical documentation for global trials, maintaining 100% accuracy in metadata, completeness, and sponsor-guideline compliance. I coordinate with sponsors, CROs, and internal teams to resolve discrepancies and keep concurrent workstreams moving under strict deadlines.
Previously at Himedia Laboratories, I maintained GLP-compliant QC logs, batch records, and deviation reports while researching process issues and documenting corrective actions. I also support teams with clear process guidelines, technical research, and consistent documentation standards.
Experience
Work history, roles, and key accomplishments
Processed and validated high volumes of clinical documentation for global trials, ensuring 100% accuracy in metadata, completeness, and compliance with sponsor guidelines. Coordinated with sponsors, CROs, and internal teams to resolve discrepancies and drafted process notes to support team members.
Education
Degrees, certifications, and relevant coursework
Mumbai University
Master of Science, Biotechnology
Grade: 9.5 CGPA
Pursued a Master of Science in Biotechnology, achieving a CGPA of 9.5.
Tech stack
Software and tools used professionally
Availability
Location
IndiaAuthorized to work in
Salary expectations
Job categories
Skills
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