Philadelphia, PA5 days ago
Timely and accurately completes all documentation assigned, including source documentation in study or clinic charts, collected of Informed Consent Form including ICF checklists, electronic case report forms and data entry; resolves and responds to queries from the study sponsor and regulatory agencies in a timely manner under the direction of the Research Director, with mentorship from Sr. Reports AEs, SAEs, and Special Situations in accordance with clinical trial agreements, FIGHT Research SOPs, and ICH GCP, to the PI and Research Director for timely submission to the FIGHT IRB, study sponsor, and any applicable federal regulatory agencies.