Merck is seeking a Clinical Research Associate (CRA) to lead site management and monitoring across assigned protocols within the UK nationwide. You will ensure compliance with ICH/GCP, regulatory requirements, and sponsor SOPs, while collaborating with global and regional teams.
The role involves building strong investigative site partnerships, performing remote and on-site visits, maintaining CTMS/eTMF documentation, and supporting audits.
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Clinical Research Associate | Global Site Monitoring Lead employer: Merck
Join a dynamic team in Livingston where innovation meets inclusivity! As a Production Operator in our cleanroom, you'll benefit from a supportive work culture that values diverse perspectives and fosters personal growth. With opportunities for professional development and a commitment to employee well-being, we empower you to make a meaningful impact in the fields of Healthcare, Life Science, and Electronics.
