leader with extensive experience in human subjects research protections, federal program management, and quality assurance.... Roles and Responsibilities: Serve as the Program Manager for a DHS contract supporting research compliance and oversight...
The Clinical Research Program Manager will serve as a senior clinical research professional and is responsible... and policies governing clinical research involving protection of human subjects (JCAHO, FDA, ICH, GCP, OHRP, IRB, NIH). Function...
research subjects. Key responsibilities include: Serving as alternate/deputy Program Manager during any absence of the... Assurance Program Office Human Research Protections Group (HRPG) to ensure departmental compliance with federal regulations...
using their preferred program and analyze results. The research coordinator will work as part of a highly collaborative team... Coordinator will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections...
) and guidance (International Counsel on Harmonization) regarding human subjects research and use of protected health information... of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration...
) and guidance (International Counsel on Harmonization) regarding human subjects research and use of protected health information... of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration...
human subjects research and use of protected health information. Uses research funds and resources appropriately... of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration...
) and guidance (International Counsel on Harmonization) regarding human subjects research and use of protected health information... of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration...