Job Summary
The role of the Clinical Research Associate in Early Clinical Development involves joining our expanding team at IQVIA, based in Durham, North Carolina. This position is essential for supporting clinical trials by ensuring adherence to regulatory requirements and maintaining essential documentation.
Responsibilities
- Monitor clinical studies to guarantee compliance with protocols and regulatory obligations.
- Oversee documentation within both the Trial Master File (TMF) and Investigator Site File (ISF).
- Coordinate and liaise with trial sites to promote effective communication and project progress.
Qualifications
- Prior experience in clinical research or a related field is preferred.
- Strong understanding of regulatory standards and clinical trial management.
- Excellent organizational skills and attention to detail.
