Job Overview

Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning.

Essential Functions

• 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 purpo...