Raminder Pathak, MD
About Raminder Pathak, MD
Raminder Pathak, MD, is the Senior Director and Medical Safety Assessment Physician at Bristol Myers Squibb in New Jersey, United States. He has extensive experience in pharmacovigilance, clinical research, and regulatory compliance, having previously held various roles at Bristol Myers Squibb, MD Anderson Cancer Center, Texas Heart Institute, and All India Institute of Medical Sciences.
Current Role at Bristol Myers Squibb
Raminder Pathak, MD is currently employed as a Senior Director, Medical Safety Assessment Physician at Bristol Myers Squibb in New Jersey, United States. In this role, he ensures the safety and regulatory compliance of clinical programs. His responsibilities include submitting periodic reports to the Food and Drug Administration, developing Safety Data Exchange Agreements (SDEAs), and providing medical and clinical guidance to oncology and immuno-oncology clinical programs.
Career at Bristol Myers Squibb
Dr. Pathak has held various positions at Bristol Myers Squibb over the years. Before his current role, he served as the Therapeutic Area Head, Solid Tumor Pharmacovigilance in 2020 for five months. Prior to this, he worked as a Director for ten years, from 2010 to 2020. In all these roles, he has consistently contributed to ensuring the safety and compliance of clinical trials and product development processes.
Previous Positions and Experience
Raminder Pathak, MD has accumulated diverse experience in the medical field. He previously worked at MD Anderson Cancer Center in Experimental Therapeutics and Phase I Clinical Trials for eight months in 2007-2008. Prior to that, he served as a Clinical Observer at Texas Heart Institute for ten months in 2007. His early career includes a seven-year tenure as a Clinical Research Officer at All India Institute of Medical Sciences from 1993 to 2000.
Educational Background
Dr. Pathak achieved his MD in Medicine from Punjabi University, Patiala, where he studied from 1987 to 1993. He also holds a certificate from ECFMG. His strong academic foundation has been instrumental in his medical career, enabling him to take on complex roles and responsibilities in clinical research and medical safety assessment.
Key Contributions and Roles
Throughout his career, Raminder Pathak, MD has made significant contributions in the field of medical safety and pharmacovigilance. He has chaired the Safety Management Team, acted as a medical expert during product development, and remediated pharmacovigilance deficiencies found during audits. Additionally, he has addressed labeling concerns, interpreted regulatory mandates, and ensured compliance with foreign regulatory requirements for clinical and post-marketing adverse event filings.