Swapnil Pandey
Leader in Global Clinical Trial Management & Delivery/ Global Clinical Development- Oncology and Hematology
- Role
- Executive Director, Clinical Trial Management at Medpace
- Location
- Cincinnati, OH, US
- LinkedIn followers
- 500 followers
About Swapnil Pandey
Execution-focused, leader of global clinical trials with over 20 years of experience in project management and operational delivery in the CRO industry across a broad range of Oncology and Hematology therapeutic areas, varying from early phase studies to large global registration trials, with overall responsibility for operational and financial delivery, as well as customer relationship interface. Proven track record in setting up and driving strategic partnerships with SMID/Biotech as well as large pharma clients in delivering on portfolios and programs of clinical trials, thereby driving repeat business. Excel in collaborating with vendor partners, AROs/ACROs, and specialized cooperative groups- all with the ultimate goal of ensuring successful project delivery. Additionally, I oversee and strategize new business initiatives, including proposal and budget development, and lead impactful proposal defense meetings. I bring over 12 years of experience in line management and mentorship, specializing in talent acquisition and nurturing top talent to ensure they thrive and contribute significantly to the organization\'s success.
Experience
Executive Director, Clinical Trial Management
Feb 2025 — Present · Cincinnati, OH, US
Education
University of Cincinnati
Master of Science, Clinical Research and Drug Development
2006 — 2008
University of Cincinnati
Master of Science, Applied Industrial Statistics
2002 — 2005
Pandit Ravishankar Shukla University
Bachelor of Science/ Bachelor of Engineering, Mechanical Engineering
1996 — 2000
Skills
- Clinical Research
- Regulatory Affairs
- Project Management
- Cross-Functional Team Leadership
- Electronic Data Capture (Edc)
- Hematology
- Operations Management
- Program Management
- Phase I
- Oncology
- Protocol
- Data Management
- 21 Cfr Part 11
- Sas
- CRO Management
- Edc
- Therapeutic Areas
- Ctms
- U.s. Title 21 Cfr Part 11 Regulation
- Biostatistics
- Clinical Trial Management System (Ctms)
- Regulatory Submissions
- CRO
- Clinical Development
- Clinical Trials
- Pharmaceutical Industry
- Sop
- Fda
- U.s. Food and Drug Administration (Fda)
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