Morgan Mathis Email & Phone Number

Wilmington, Nc, Us

Wilmington, Nc, Us

Wilmington, North Carolina, United States

•Verify that the rights and well-being of subjects are protected, the reported trial data are accurate, complete, and verifiable from source documents, and the conduct of the trial is in compliance with the currently approved protocol, GCP, and applicable regulatory requirements; •Ensure site compliance while conducting qualification, study initiation, routine monitoring, and study site close-out visits for research sites according to Medpace/Sponsor SOPs;•Serve as the primary resource to the clinical investigator and site staff;•Maintain close collaboration, interaction, and effective working relationships with Medpace internal cross-functional teams;•Ensure quality completion of visit reports, follow-up letters, and maintenance of study-related databases;

Wilmington, North Carolina, United States

Responsible for onsite and remote monitoring activities in accordance with ICH-GCP, applicable regulations, and study processes. Verifies the protection of study participants, ensures integrity of clinical data, and ensures the study is conducted in compliance with the approved protocol, GCP, and applicable regulations. Verifies proper management and accountability of IP. Additional responsibilities include writing trip reports of site findings and escalating deficiencies as appropriate.

Wilmington, North Carolina, United States

Responsible for onsite and remote monitoring activities in accordance with ICH-GCP, applicable regulations, and study processes. Verifies the protection of study participants, ensures integrity of clinical data, and ensures the study is conducted in compliance with the approved protocol, GCP, and applicable regulations. Verifies proper management and accountability of IP. Additional responsibilities include writing trip reports of site findings and escalating deficiencies as appropriate.

Wilmington, North Carolina, United States

Responsible for supporting site start-up activities, including site recruitment, collection and review of essential documents, reviewing and approving ICF’s, assisting sites with IRB/IEC submission, and site activation.

Wilmington, North Carolina, United States

Responsible for supporting site start-up activities, including site recruitment, collection and review of essential documents, reviewing and approving ICF’s, assisting sites with IRB/IEC submission, and site activation.

Wilmington, North Carolina, United States

Responsible for supporting site start-up activities, including site recruitment, collection and review of essential documents, reviewing and approving ICF’s, assisting sites with IRB/IEC submission, and site activation.

Wilmington, North Carolina, United States

Wilmington, North Carolina, United States

United States