Varun Garg
VP, Clinical Pharmacology at PureTech Health
- Role
- Vice President, Clinical Pharmacology at Puretech Health
- Location
- Boston, MA, US
- LinkedIn followers
- 500 followers
About Varun Garg
Experienced drug development professional, especially in the fields of Antivirals, Cystic Fibrosis, CNS, and Oncology. Lead Clinical Pharmacologist responsible for filing and approval of SYMDEKO (tezacaftor/ivacaftor combination for CF, approved in 2018) and INCIVEK (Telaprevir for HCV, 2011), LEXIVA (fosamprenavir for HIV) NDAs. Successful defense of INCIVEK at the antiviral advisory committee meeting in April 2011. Member of the Vertex-GSK joint drug development committee for LEXIVA (fosamprenavir). Founding member of organizing committee for the International Workshop for the Clinical Pharmacology of Hepatitis Therapy (20••••12). Specialties: Clinical Pharmacology, Pharmacokinetics, Pharmacodynamics, PK/PD Modeling and Simulation applied to drug development, Drug Interactions, Infectious Disease, Cystic Fibrosis, Oncology, Antivirals, Due diligence and Business Development support.
Experience
Vice President, Clinical Pharmacology
Jun 2022 — Present · Boston, MA, US
Education
University at Buffalo
Ph.D., Pharmaceutics
University of Rhode Island
MS, Pharmaceutics
Indian Institute of Technology, Varanasi
BS, Pharmaceutical Sciences
Skills
- Adme
- Winnonlin
- Clinical Development
- Regulatory Submissions
- In Vivo
- Pk
- Clinical Research
- Clinical Pharmacology
- CRO Management
- Dmpk
- Clinical Study Design
- Biotechnology
- Drug Metabolism
- New Drug Application (Nda)
- Drug Delivery
- Pharmacokinetics
- Pharmacodynamics
- Antiviral
- Ind
- Pharmaceutical Industry
- Nonmem
- Translational Medicine
- Pk/Pd
- Pharmacology
- Drug Development
- Virology
- Nda
- Clinical Trials
- Drug Interactions
- CRO
- Pharmaceutical Research
- Pharmacometrics
- Oncology
- Biomarkers
- Infectious Diseases
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