Clinical Research Coordinator, Oncology Research, Full Time, Days

Job description

Inspire health. Serve with compassion. Be the difference. Job Summary: Assists with screening, consents, enrollment and maintaining research subjects as well as maintain compliance to research protocols. Acts as the liaison between monitors, investigators and study personnel regarding all data management for patients enrolled in clinical trials. Responsible for abstraction of accurate, complete and timely data from the medical record, as needed. Maintains protocol regulatory documents in compliance with standard operating procedures (SOPs). Provides a safe environment for patients, families and clinical staff. Essential Functions: All team members are expected to be knowledgeable and compliant with Prisma Health's purpose: Inspire health. Serve with compassion. Be the difference. Compiles medical records of research subjects during the on-study, treatment and follow-up periods and reports required elements to the research sponsor in a complete, accurate and timely manner. Ensures protocol compliance and accurate data submissions during the treatment and post treatment phase of a research trial. Ensures that research tasks are completed correctly by referencing the most current copy...