Paul Onuoha Email & Phone Number

Summit, New Jersey, Us

- To make sure that the safety and well being trial subjects are protected- Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelines- Conduct site selection visits, initiation, routine, and close-out visits at investigator sites. - Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelines- Ensure accuracy of 1572 information, and ensure shipment of study-related materials.- Verify source to CRF’s and ensure accuracy; also ensure that corrections are made.- Monitor investigator sites for compliance in reporting AE and SAE

To make sure that the safety and well being trial subjects are protectedMonitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesConduct site selection visits, initiation, routine, and close-out visits at investigator sites. Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesEnsure accuracy of 1572 information, and ensure shipment of study-related materials.Verify source to CRF's and ensure accuracy; also ensure that corrections are made.Monitor investigator sites for compliance in reporting AE and SAE

Los Angeles, Ca, Us

To make sure that the safety and well being trial subjects are protectedMonitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesConduct site selection visits, initiation, routine, and close-out visits at investigator sites. Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesEnsure accuracy of 1572 information, and ensure shipment of study-related materials.Verify source to CRF's and ensure accuracy; also ensure that corrections are made.Monitor investigator sites for compliance in reporting AE and SAE

Los Angeles, Ca, Us

- To make sure that the safety and well being trial subjects are protected- Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelines- Conduct site selection visits, initiation, routine, and close-out visits at investigator sites. - Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelines- Ensure accuracy of 1572 information, and ensure shipment of study-related materials.- Verify source to CRF’s and ensure accuracy; also ensure that corrections are made.- Monitor investigator sites for compliance in reporting AE and SAE

Princeton, New Jersey, Us

To make sure that the safety and well being trial subjects are protectedMonitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesConduct site selection visits, initiation, routine, and close-out visits at investigator sites. Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesEnsure accuracy of 1572 information, and ensure shipment of study-related materials.Verify source to CRF's and ensure accuracy; also ensure that corrections are made.Monitor investigator sites for compliance in reporting AE and SAE

Merthyr Tydfil, Wales, Gb

Conduct site selection visits, initiation, routine, and close-out visits at investigator sites. Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesEnsure accuracy of 1572 information, and ensure shipment of study-related materials.Train site staff on protocol issues that arise frequently.Close all outstanding queries during a close out visit.Communicated trial progress to the project team on a monthly basis.

Mshs, Clinical Research Administration

Ba, Information System

Mshs, Clinical Research Management