Gail Hoffmann Email & Phone Number

Tampa, Fl, Us

Perform quality control, reconciliation, and in-house auditing of clinical trials documentation at every study phase to ensure FDA compliance.* Compile, edit, and enter data to be rolled out from the company to clinicaltrials.gov and other public domains.* Manage access to proprietary portals and Web sites for study investigators including doctors, pharmacists, and CRO (Client Research Organization) staff.* Track and amend important milestones and drivers (first/last patient treated, number of labs affiliated with the research, etc.) per country and site, including setting drug shipment dates and other vital markers for the successful completion of the trial/facilitation of overall drug approval.* Copyedit Protocol departmental documentation.