Clinical Research Associate (REMOTE)
Please note that this is a 12 to 18-month contract position. Veeva experience is required. Notes from the Manager: • It can be fully remote but must work in PST timezone. • For this position, it is more of a specialist role, so their day-to-day won t be typical. • The ideal candidate for this role would have at least 5 years of experience as a CRA and may already have some CTM experience. • It will also help if they have some QA experience. • Clinical coordinators would not work. Job Posting Qualifications • Bachelor's or Master's Degree or equivalent. • Post-graduate, certification, and/or license may be required. • Typically, at least 3 - 5+ years relevant experience. Job Posting Description Responsible for overall clinical study management, including planning, communication, coordination and practical tasks for the studies. • Coordinates Ethical Committee and Institutional Review Board notifications. • Creates, maintains and oversees study files and archiving. • Manages testing laboratories including selection of laboratories for the studies. • Manages clinical research organizations and ensures monitoring of studies, data collection and handling. • Prepares, revises and maintains procedures for the conducting of clinical studies. Applicants must provide their phone number. Reference job number A5017 Apply tot his job