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Clinical Research Coordinator, Full-Time, Days - Greenville, United States - Prisma Health
Description
Inspire health. Serve with compassion. Be the difference.Job Summary
Under minimal supervision, 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 SOPs. Provides a safe environment for patients, families and clinical staff.Accountabilities
This is a non-management job that will report to a supervisor, manager, director or executive.
Minimum Education
Associate's Degree- Clinical, healthcare or scientific related field required
Minimum Experience
3 years- Allied health, medical or research related experience
In lieu of the Above Minimum Requirements
BS degree in clinical, healthcare or scientific related field required and 1 yr of experience
Other Required Experience
SoCRA or ACRP certification- Preferred
Oncology medical research experience- Preferred
Some medical office experience preferable in oncology- Preferred
Medical terminology knowledge- Preferred
Work Shift
Day (United States of America)
Location
Cancer Centers - Faris Road
Facility
1008 Greenville Memorial Hospital
Department
OP Oncology Research-CIF
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