USA (North Carolina) – Global – Clinical Trials Associate Consultant Services

(1) Vendor needs to provide clinical trials associate consultant services to the government authority located in North Carolina.- Perform clinical research closeout activities for four multi-site clinical research studies with senior research staff.- Assist clinical research teams, specifically the protocol specialist, in closeout by assisting with already shared study site closeout checklists, maintaining filing and tracking systems to coordinate essential regulatory documents for study closeout, drafting and issuing meeting minutes, and facilitating communication.- Provide overall administrative support to the clinical research team.- Maintaining shared filing systems (e.g., SharePoint, MS Teams) and collecting, reviewing, and filing essential regulatory documents.- Communicating directly with assigned study sites to provide assistance, collect required documents, seek site updates, consulting with protocol specialists as needed.(2) All questions must be submitted no later than 22 June 2026.

Onshore (USA Organization Only);

Performance of the work will be Offsite.