IQVIA is seeking a Clinical Research Coordinator to support clinical research studies and ensure the highest standards of care and compliance.
Requirements
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Phlebotomy is required; pediatric experience is highly preferred.
- Strong attention to detail
- Ability to establish effective working relationships
- Minimum 1 year of relevant work experience in clinical research (preferred)
- High School Diploma or equivalent education and experience
- Knowledge of ECG, spirometry, sample collection, and vital signs
Responsibilities
- Perform a variety of complex clinical procedures, including ECG, spirometry, 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.
- 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 volunteer advocate and maintain a safe environment in accordance with Health and Safety policies.
- Recruit, screen, and orient volunteers, ensuring their safety and well-being throughout the study.
Other
- High School Diploma or equivalent education and experience
- Minimum 1 year of relevant work experience in clinical research (preferred)
- Strong attention to detail and ability to establish effective working relationships
- This position is not eligible for sponsorship
- Full-time, 40 hours per week
