Description
IQVIA is hiring a Senior Clinical Research Associate 1 to perform monitoring and site management work, ensuring sites conduct studies and report data according to the study protocol, regulations, and sponsor requirements.
The role involves:
- Conducting site monitoring visits, including selection, initiation, monitoring, and close-out visits
- Working with sites to adapt and drive subject recruitment plans
- Providing protocol and study training to assigned sites
- Evaluating study site practices and escalating quality issues
- Managing study progress, tracking regulatory submissions, and resolving data queries
- Maintaining documentation and verifying site files
Requirements include:
- Bachelor's degree in a scientific discipline or healthcare
- At least 2 years of on-site monitoring experience
- Knowledge of clinical research regulatory requirements and Good Clinical Practice (GCP)
- Therapeutic and protocol knowledge (provided in company training)
The potential base pay range for this role is $90,200.00 - $175,100.00 per year.