Tarit K. Banerjee, M.D.

Tarit K. Banerjee, MD has recently retired as Oncology Research Director at Marshfield Clinic, Marshfield, WI. Dr. Banerjee has served as a Clinical Associate Professor in Medicine at the University School of Medicine and Public Health, Madison, WI, Assistant Medical Director of Hospice Program of St. Joseph`s Hospital of Marshfield, WI, and Clinical Associate of Oncology at Edmonton, University Hospital of Alberta, Canada. He had been associated with ECOG since 1974 and had been Principal Investigator of NCI awarded Marshfield CCOP since 1983 until his retirement. During his years at Marshfield, Dr. Banerjee also participated with NSABP, RTOG, GOG, COG, URCC, MD Anderson CCOP and with Cancer Treatment and Cancer Control Protocol Studies. He also took part as a member in the executive committee of MDA CCOP and was a member of ECOG Symptom Control Consortium. His particular interest includes solid tumor malignancy and cancer control research aimed at improving quality of life, symptom control and cancer prevention.

Dr. Banerjee received his medical degree at Calcutta National Medical College, India. He completed his rotating internship in New Delhi, India, Medical Residency in Lutheran/Cleveland Metro General Hospital, Cleveland, Ohio, and Cancer Research Fellowship at Roswell Park Memorial Institute, Buffalo, N.Y.  He is Board Certified in Internal Medicine and Medical Oncology. He received his Fellowship of the American College of Physicians and the Royal College of Physicians of Canada (FRCP-C) by written and oral examination. He is emeritus member of American College of Physicians and American Society of Clinical Oncology as well as lifetime member of Indian Medical Association. He had received several recognitions from regional division of American Cancer Society, NCI, ECOG, NSABP, MD Anderson CCOP, for his contribution in advancing cancer treatment and cancer control clinical trials in the community setting. In his early career he performed research in leukocyte mobilization in normal and diseased subjects as well as human tumor cell clonogenic assay.

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