Base: $71,900.00 - $119,900.00; bonus/equity: not ...
Not specified (assumed to be hybrid based on typical industry practices).
On-site monitoring experience
Oncology solid tumor monitoring
Ensure compliance with gcp/ich
IQVIA Biotech is seeking a Clinical Research Associate I (CRA I) with a minimum of 6 months of on-site monitoring experience, specifically in oncology solid tumors. The role focuses on site monitoring and management to ensure compliance with clinical research protocols and regulations
Job Summary
The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities.
You will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines.
Accurate and timely documentation is critical, and the CRA I prepares detailed monitoring visit reports, follow-up letters, and all required study documentation to ensure audit readiness and transparent oversight.
Matching Summary
Match Score: 75
IQVIA Biotech is seeking a Clinical Research Associate I (CRA I) with a minimum of 6 months of on-site monitoring experience, specifically in oncology solid tumors. The role focuses on site monitoring and management to ensure compliance with clinical research protocols and regulations.
Salary
Base: $71,900.00 - $119,900.00; Bonus/Equity: Not specified; Benefits: Range of health and welfare and/or other benefits