Coord-Clinical Research
About The Position
Clinical Research Coordinator assumes responsibility for the overall coordination of research trials from all aspects. This position will be responsible for identifying clinical trials, feasibility reviews and study activation. Screens for potential patients for clinical trial opportunities, educating patients and families about research and, obtaining and developing research data, and monitoring compliance with research protocols. Responsible for study coordination and study implementation in collaboration with the participating physicians, their staff, regulatory staff and study sponsor. Maintains strong communication with physicians, nurses, pharmacy and other key persons regarding available protocols. Maintains protocol integrity through adherence of protocol requirements. Responsible for data management as required per protocol. Must be self-starter/motivated, detail-oriented, willing to develop the clinical research service line within hospital system. Knowledge of nursing practices preferred. Willing to learn and train on required clinical research database and clinical trial management system.
Requirements
- BSN with minimum of two years clinical experience OR Bachelors (BA, BS, BSN) and two years in clinical and/or clinical research experience OR Associate Degree Nursing (ADN), RN, with minimum of four years clinical experience OR Current certification in clinical research (SOCRA-CCRP, ACRP-CCRC or ACRP-CP) with three years clinical research experience with human subjects
- Current South Carolina RN license (for nurse applicants only)
- Must have own transportation to other hospitals and doctors' offices
- Must be flexible in responsibilities and work schedule
- Must be meticulous with detail
- Must be able to read, write, and speak English fluently
- Must have good communication skills
- Must be able to respond calmly and efficiently in high stress situations
- Must be able to sit for long periods of time, filling out paperwork
- Must be self-directed and able to work without supervisor
Nice To Haves
- Knowledge of nursing practices preferred
- Willing to learn and train on required clinical research database and clinical trial management system
- Master's in a Heath Related field or Bachelor of Science in Nursing
- One (1) year oncology experience
- Clinical research experience
- Certification in research (CCRC, CCRP)
- Membership in a Clinical Research Professional organization (ACRP, SoCRA, etc.) within 1 year of hire or as eligible based on research experience
Responsibilities
- Identifying clinical trials
- Feasibility reviews
- Study activation
- Screening for potential patients for clinical trial opportunities
- Educating patients and families about research
- Obtaining and developing research data
- Monitoring compliance with research protocols
- Study coordination and study implementation in collaboration with the participating physicians, their staff, regulatory staff and study sponsor
- Maintaining strong communication with physicians, nurses, pharmacy and other key persons regarding available protocols
- Maintaining protocol integrity through adherence of protocol requirements
- Data management as required per protocol
- Working as a team member with other Research staff, doctors, departments, community, and other components
- Attending research meetings
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
