Description
Worldwide Clinical Trials is hiring a Clinical Research Associate to manage clinical trial sites from qualification through close-out, including monitoring, site management, documentation, safety and consent review, source data verification, CRF review, query resolution, and Trial Master File updates. The role requires oncology experience, at least two years of CRA experience, a four-year university degree or RN/BSN in Nursing, proficiency with Microsoft Office, CTMS, and EDC systems, strong communication and organizational skills, independent work ability, and willingness to travel.
