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Clinical Research Coordinator
2 months ago
We are seeking a highly skilled and detail-oriented Clinical Research Coordinator to join our team at Bon Secours Mercy Health. As a Clinical Research Coordinator, you will play a critical role in the coordination and management of clinical research studies, ensuring the highest level of quality and compliance.
Key Responsibilities- Recruit and screen study participants, ensuring they meet the protocol requirements
- Coordinate and manage research studies, including protocol development, informed consent, and data collection
- Work closely with investigators, research staff, and other departments to ensure seamless study execution
- Maintain accurate and detailed research files, including study protocols, informed consent documents, and participant data
- Collaborate with regulatory agencies and sponsors to ensure compliance with federal regulations and guidelines
- 2-year associate's degree in nursing or related field
- Current RN license from the state of Ohio
- Minimum 3-5 years of recent clinical experience, preferably in critical care
- Ability to write, follow, and monitor study protocols, recruit and consent study subjects, collect and enter data, and follow institutional policies, FDA regulations, and ICH/GCP guidelines
Bon Secours Mercy Health offers a comprehensive benefits package, including medical, dental, and vision plans, flexible spending accounts, life insurance, and retirement savings plan. We also offer paid time off, educational assistance, and a supportive work environment.
We are an equal opportunity employer and welcome applications from diverse candidates. If you are an individual with a disability and require a reasonable accommodation, please contact our Talent Acquisition Team.