... and close-out visits) in accordance with contracted scope of work and Good Clinical Practice ... . • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol ...

... regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization ... issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of ...

... Role Overview: As a Clinical Research Associate, you’ll be at the forefront of ensuring our ... , monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) and International ...

... IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring ... requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines ...

... Clinical Practice. • Work with sites to adapt, drive, and track subject recruitment plan in line with ... issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of ...

... training to assigned sites Evaluating the quality and integrity of site practices – escalating quality ... knowledge of applicable clinical research regulatory requirements.You should have: A Bachelor ...

... regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization ... issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of ...

... quality and integrity of site practices – escalating quality issues as appropriate Managing progress ... colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research ...

... training to assigned sites Evaluating the quality and integrity of site practices – escalating quality ... knowledge of applicable clinical research regulatory requirements.You should have: A Bachelor ...