Clinical Research Coordinator - Cincinnati, OH
IQVIA•Parsippany, OH
•Onsite
About The Position
We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Requirements
- Bachelor’s degree preferred or equivalent combination of education and relevant experience.
- Minimum 1+ years of relevant work experience in clinical research.
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Strong attention to detail and ability to establish effective working relationships.
- Proficiency with EDC systems , data entry accuracy, and query management.
Responsibilities
- Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
- Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
- Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
- Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
- Collect and accurately record clinical data in case report forms (CRFs).
- Collaborate with investigators and monitors, addressing queries and ensuring data quality.
- Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.
Benefits
- health and welfare and/or other benefits
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
