Clinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-Site

The Clinical Research Coordinator II supports clinical trials through participant recruitment and screening, conducting informed consent, and coordinating protocol-required visits and procedures. Responsibilities include ensuring accurate data collection and quality review, maintaining regulatory documentation, assisting with IRB submissions, and monitoring adverse events. This role requires strong organizational and communication skills to ensure protocol compliance and participant safety. A Bachelor’s degree or equivalent experience with at least two years in research activities is required, along with basic life support certification.