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AMR has an expert staff comprised of our Clinic Administrator who manages budgeting of our research trials, eleven experienced Clinical Research Coordinators, LVN, MA, phlebotomist and pharmacy technician. Most of our staff is IATA certified for shipping hazardous materials.

Dr. Eric J. Lawitz is board certified in Gastroenterology and Internal Medicine and is the Medical Director and Principal Investigator for AMR.  Dr. Lawitz has been conducting clinical trials for 12 years, has conducted extensive research in Chronic Hepatitis C and is a Certified Physician Investigator.  He has been both an investigator and sponsor/investigator. Dr. Lawitz has extensive experience in Internal Medicine and Gastroenterology.

Dr. K.P. Ganeshappa is board certified in Gastroenterology and Internal Medicine and is a sub-investigator.  Dr. Ganeshappa has extensive experience in Gastroenterology since 1971.  He has extensive experience conducting numerous clinical trials investigating GERD, and has participated in Chronic Hepatitis C clinical trials since 2000.

Dr. Hector D. Allende is board certified in Gastroenterology and Internal Medicine is a sub-investigator.  Dr. Allende has extensive experience in Gastroenterology and has been participating in clinical trials, which emphasis in IBS and GERD, since 1981.

Dr. Ravi Botla is board certified in Gastroenterology and Internal Medicine and is a sub-investigator.  Dr. Botla has extensive experience in Gastroenterology and has been participating in clinical trials, with emphasis in liver disease, since 1995.
Dr. Ravi Ganeshappa is board certified in Gastroenterology and Internal Medicine is a sub-investigator. Dr. Ganeshappa has been participating in clinical trials, with emphasis in Barrett's Esophagus, since 1989.
PA. Michael R. France, MPAS has experience as a clinical research sub-investigator, with emphasis in Chronic Hepatitis C, since 2000, and is a Certified Clinical Research Coordinator.  He has over 22 years of experience in Family and Emergency Medicine and Otorhinolaryngology.

All investigators are trained and experienced in all facets of clinical research to include: Good Clinical Practices, Investigator Responsibilities, Documentation, Reporting of AEs and SAEs, working with IRBs and CRFs.

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