Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
Review study protocols, Case Report Forms (CRFs), other study‑specific documents, and electronic data capture systems used to record clinical research data;
Attend all relevant study meetings;
Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research;
Recruit and screen patients for clinical trials and maintain subject screening logs;
Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits;
Design and maintain source documentation based on protocol requirements;
Schedule and execute study visits and perform study procedures;
Collect, record and maintain research subject study data accordi...