Clinical Research Associate II
On-siteLivingston, Scotland, United Kingdom
Job Summary
Conduct site monitoring visits for interventional studies, including selection, initiation, monitoring, and close-out, ensuring adherence to Good Clinical Practice and ICH guidelines. Adapt and track subject recruitment plans, administer protocol training, and evaluate site practices for regulatory compliance. Manage study progress by tracking regulatory submissions, enrollment, case report form completion, and data query resolution. Maintain Trial Master File and Investigator's Site File documentation, submit visit reports, and collaborate with the study team. Requires two years of on-site monitoring experience and full UK right to work. Join IQVIA's cFSP team in Scotland to accelerate innovation for a healthier world.
Required Qualifications
- At least 2 years on-site monitoring experience of interventional studies
- Degree in scientific discipline or health care or equivalent industry experience
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Ability to establish and maintain effective working relationships with coworkers and clients
- Full UK right to work required, this position is not eligible for visa sponsorship
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