Denis Ntivunwa Email & Phone Number | Over 14 years of international multi-therapeutic clinical trials as well as management of investigative sites including site selection, start-up activities, initiation, routine and close out monitoring visits. Therapeutic experience in the following areas: Central Nervous System (mental disorders, Alzheimer’s disease), Oncology, Infectious Diseases (HIV/AIDS), Dermatology, Cardiovascular, Endocrinology, Urology and Vaccines. Certified Clinical Research Professional (CCRP) from the Society of Clinical Research Associates (SoCRA, Chalfont, PA 18914 USA) on July 2008 Specialties: •Knowledge of the ICH-GCP guidelines and FDA regulations relating to Good Clinical Practice and Clinical Trials •Knowledge of medical terminology and the local regulations for clinical trials •Competent with Microsoft Office, CTMS, EDC and Lotus Notes •Knowledge of Drug Discovery and Development Process

Denis Ntivunwa

Over 14 years of international multi-therapeutic clinical trials as well as management of investigat...
Miami, Florida, United States

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Denis Ntivunwa’s Email dntivunwa@iconplc.com

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Denis Ntivunwa’s Location Miami, Florida, United States

Denis Ntivunwa’s Current Industry Pra Health Sciences

Denis Ntivunwa’s Prior Industry Jansen Cilag

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Senior Clinical Research Associate

2008-01-01 00:00:00 - Present

Medical Affair Associate

2005-01-01 00:00:00 - 2007-01-01 00:00:00

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Denis Ntivunwa is a Over 14 years of international multi-therapeutic clinical trials as well as management of investigative sites including site selection, start-up activities, initiation, routine and close out monitoring visits. Therapeutic experience in the following areas: Central Nervous System (mental disorders, Alzheimer’s disease), Oncology, Infectious Diseases (HIV/AIDS), Dermatology, Cardiovascular, Endocrinology, Urology and Vaccines. Certified Clinical Research Professional (CCRP) from the Society of Clinical Research Associates (SoCRA, Chalfont, PA 18914 USA) on July 2008 Specialties: •Knowledge of the ICH-GCP guidelines and FDA regulations relating to Good Clinical Practice and Clinical Trials •Knowledge of medical terminology and the local regulations for clinical trials •Competent with Microsoft Office, CTMS, EDC and Lotus Notes •Knowledge of Drug Discovery and Development Process