Description
IQVIA is seeking a Clinical Research Coordinator (CRC) to join its team in Union, SC. The CRC will support clinical research studies under the supervision of a principal investigator. The role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Key Responsibilities:
- Perform various 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.
Qualifications:
- 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.
The potential base pay range for this role is $35.00-$42.00 per hour.