Hybrid in Jefferson City, Missouri
•
Today
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
Easy Apply
Contract
$20 - $24














