Bridgette Thompson Email & Phone Number

Wilmington, NC, US

• Identifying/selecting an investigator who will be responsible for the conduct of the trial at the trial site.
• Liaising with doctors/consultants or investigators on conducting the trial.
• Setting up the trial sites, which includes ensuring each center has the trial materials, including the trial drug often known as the investigational medicinal product. Training the study staff in the standard operating.
• Verify that investigator and investigator’s team are adequately trained and comply with the protocol.
• Verify that IRB/IEC operates and complies as per GCP, SOP and applicable regulatory requirements.
• Monitoring the trial throughout specified duration involving monitoring visit to the trial sites.

Atlanta, GA, US

• Independently managed significant and key aspects of a large clinical trial or all aspects of one or more small trials, or research projects. Trains and provides guidance to less experienced staff.
• Oversaw data management for research projects. Interfaced with research participants and resolves issues related to study protocols.
• Authorized purchases for supplies and equipment maintenance.
• Determined effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials.
• Periodically audited operations including laboratory procedures to ensure compliance with applicable regulations; provided leadership in identifying and implementing corrective actions/processes.
• Monitored IRB submissions and responded to requests and questions.