Mayur Kherdikar
Study Director Global Clinical Operations
- Role
- Study Director at Novartis
- Location
- Hyderabad, TG, IN
- LinkedIn followers
- 500 followers
About Mayur Kherdikar
Mayur holds double masters degree in Pharmaceutical medicine from Hibernia University and in Clinical research from Cranfield Universtiy UK. He is a bachelor of dental sciences from Maharashtra University of health sciences Nashik.Mayur started his journey in drug development at Novartis in Hyderabad in 2007 and since then over the years has moved latterly and developed robust experience across various areas of drug development such as project management, budget planning and forecasting; clinical operations and medical writing. He has a wealth of experience in design, set-up, execution and reporting of large scale global II-IV interventional and non-interventional clinical trials. He has managed and lead phase II- IV clinical studies across therapeutic areas such as cardiology, respiratory, immunology, neuroscience and oncology in various capacities.Currently Mayur is leading end-to-end trial management activities and team of trial manages based in USA, Switzerland & India.In addition, throughout his tenure at Novartis, Mayur has actively contributed as an SME in various global innovation/process improvement initiatives. Mayur is a passionate cyclist (randonneur) and has participated in multiple long distance brevet rides. He aspires to be an ultracyclist.Specialties : Project management, clinical trial operations, budget and forecasting, medical writing, people management.
Experience
Study Director
May 2024 — Present · Hyderabad, IN
Education
Maharashtra University of Health Sciences
B.D.S, Denitstry
2000 — 2005
Harvard Medical School
HMX pro pharmacology- drug discovery and development
Institute of Clinical Research India
M.Sc, Clinical Research
2005 — 2007
Hibernia College
Master of Science (M.Sc.), Pharmaceutical Medicine
2014 — 2016
Skills
- Training and Mentoring
- Clinical Development
- Clinical Study Design
- Clinical Trials
- Regulatory Affairs
- Data Management
- Drug Safety
- Drug Development
- Pharmacovigilance
- Regulatory Submissions
- Medical Writing
- Protocol
- Edc
- Therapeutic Areas
- Pharmacology
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