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Clinical Research Coordinator
2 months ago
Job Summary
The Clinical Research Coordinator will be responsible for the overall coordination of oncology research trials from all aspects. This position will be responsible for identifying clinical trials, conducting feasibility reviews, and activating studies. The successful candidate will screen for potential patients for clinical trial opportunities, educate patients and families about research, obtain and develop research data, and monitor compliance with research protocols.
Key Responsibilities
- Collaborate with participating physicians, their staff, regulatory staff, and study sponsors to ensure the successful implementation of oncology studies.
- Maintain strong communication with physicians, nurses, pharmacy, and other key personnel regarding available protocols.
- Ensure protocol integrity through adherence to protocol requirements.
- Manage data as required per protocol.
- Develop and maintain knowledge of oncology nursing practices.
Requirements
- Bachelor's degree in a health-related field or equivalent experience.
- Minimum of two years of clinical experience or two years of experience in clinical research with human subjects.
- Current South Carolina RN license (for nurse applicants only).
- Preferred: Master's degree in a health-related field, one year of oncology experience, clinical research experience, phlebotomy experience, and certification in research (CCRC, CCRP).
Core Job Responsibilities
- Membership in a Clinical Research Professional organization (ACRP, SoCRA, etc...) within one year of hire or as eligible based on research experience.
- Ability to work as a team member with other Research staff, doctors, departments, community, and other components.
- Flexibility in responsibilities and work schedule.
- Ability to travel to attend NCI meetings.
- Meticulous attention to detail.
- Excellent communication skills.
- Ability to respond calmly and efficiently in high-stress situations.