IQVIA UK’s cFSP team is seeking experienced Clinical Research Associates in Scotland to monitor interventional studies and support site management.
You will conduct site visits, ensure GCP/ICH compliance, coordinate recruitment, and maintain TMF/ISF documentation. The role requires at least 2 years on-site monitoring and a degree in a scientific discipline. This position offers flexible working options and the opportunity to contribute to cutting-edge clinical research with IQVIA.
#J-18808-LjbffrSenior Clinical Research Associate II - Flexible Working in Livingston employer: IQVIA LLC
IQVIA LLC is an exceptional employer located in the vibrant town of Livingston, Scotland, offering a dynamic work culture that prioritises scientific excellence and patient outcomes. Employees benefit from comprehensive training and development opportunities, fostering personal and professional growth within the clinical lab services sector. With a strong emphasis on teamwork and innovation, IQVIA provides a rewarding environment for those looking to make a meaningful impact in healthcare.
