Description
Worldwide Clinical Trials is hiring a Clinical Research Associate to manage site-level research activities across clinical studies, with responsibilities spanning site identification, study start-up, regulatory document collection, contract and budget support, site training, study maintenance, and closeout. The role involves conducting SIVs and ensuring compliance with informed consent, safety reporting, and regulatory requirements, with most site management performed remotely and regional travel required. Candidates need strong communication, organizational, and independent working skills, proficiency with Microsoft Office, CTMS, and EDC systems, a 4-year degree or nursing degree, and 5+ years of CRA experience, preferably with obesity or metabolic disease experience.
