Philip Breitfeld

Dr. Breitfeld has led development and project teams focusing on phase 1, Proof of Concept, and Pivotal trials in oncology. He has had pharmaceutical development experience in solid tumors (CRC, NSCLC, prostate, breast, SCCHN, pancreatic, renal cell carcinoma, gastric, GBM, and melanoma) and malignant hematology, including leading oncology development at both small biotechs and midsized global pharma companies. In his four years at IQVIA (Quintiles), he developed and led the Oncology Center of Excellence- the matrix organization that drives the long-term business agenda for oncology at IQVIA.

He earned his M.D. from the University of Rochester School of Medicine, where he completed his pediatric residency. He completed fellowships in pediatric hematology-oncology and medical informatics at Harvard Medical School and the Indiana University School of Medicine. Prior to entering the industry, he was on the faculty at Duke University Medical Center, the Indiana School of Medicine, and the University of Massachusetts Medical School.

Suggested For You

perspectives

July 22nd, 2025

Career Insights: From Military Service to Regulatory Strategy – Ritchie Patton’s Journey at MMS

regulatory intelligence

July 16th, 2025

Navigating the National Priority Review Voucher: Challenges and Solutions 

perspectives

July 15th, 2025

Smart AI, Smarter Oversight: What Sponsors Really Need from Their CRO 

perspectives

July 8th, 2025

Guidance for Working with External Data Vendors – Getting from LPLV to Database Lock Faster

perspectives

July 1st, 2025

Why Real-Time Data Access Matters (and How to Make the Most of It)

webinar

July 31st, 2025

Design, Data, and Decisions in Oncology Trials

perspectives

June 24th, 2025

Why Now Is the Time for Specialized, Data-Focused CRO Partners

news

June 19th, 2025

MMS Wins in the 2025 Fierce CRO Awards for Excellence in Client Service and Partnership and Dr. Uma Sharma Named CRO Champion 

perspectives

June 17th, 2025

Solving Data Complexity with Real-Time Insights, Predictive AI, and Smarter Decision-Making with Datacise

regulatory intelligence

June 16th, 2025

Key MedDRA Coding Gaps Highlighted at the ISCTM 2025 Scientific Meeting

perspectives

June 10th, 2025

Applying Artificial Intelligence (AI) and Real-World Evidence to Boost Efficiency in Patient Safety Narratives 

perspectives

June 3rd, 2025

Choosing the Right Strategy: Parallel, Sequential, and Staggered Regulatory Submissions