Tanvi Chugh
Associate director, GPS Safety Management
- Role
- Associate Director at Eli Lilly and Company
- Location
- Bengaluru, KA, IN
- LinkedIn followers
- 500 followers
About Tanvi Chugh
I am a highly skilled Pharmacovigilance (PV) expert with over 12 years of experience in the field coupled with 2 years of experience in clinical research. I have successfully managed all types of ICSRs: spontaneous, solicited, and clinical trial (including QC). I have profound experience in people management and project management, particularly for big pharma clients, leading a team of over 20 professionals for a span of 8 years. I have consistently succeeded in setting up the project from the start, transition management, implementing new operational processes and workflows, ramping up the team, setting up a governance structure, and achieving a steady state for the process in addition to driving rapid revenue growth and new business. This experience has contributed to my expertise in handling complex client projects. With a comprehensive PV background, clinical research experience, people management skills and project management acumen, I am well-equipped to make a significant impact in the pharmaceutical industry.
Experience
Associate Director
Oct 2025 — Present · Bengaluru, IN
Education
Cranfield University
Master of Science (M.Sc.), Clinical Research
2009 — 2011
Kurukshetra University, Haryana
Bachelor of Science (B.Sc.), Medical with Biotechnology
2006 — 2009
Skills
- Pharmaceutical Industry
- Sop
- Drug Safety
- Regulatory Affairs
- Lifesciences
- Clinical Research
- Clinical Pharmacology
- Clinical Trials
- Oncology
- Protocol
- Pharmacovigilance
- Cancer
- Gcp
- Ich-Gcp
- Patient Recruitment
- Edc
- Pharmacology
- Ctms
- Clinical Development
- Medical Writing
- Clinical Data Management
- Oracle Clinical
- Clinical Monitoring
- Regulatory Submissions
- Irb
- CRO
- Meddra
- Inform
- Clinical Study Design
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