Parexel International seeks a Site Activation Partner to join our UK team on a temporary basis (initially 6 months). You will lead and support site activation activities, manage essential regulatory documents, IRB submissions, and trial master file maintenance while coordinating with investigator sites and cross‑functional study teams.
This role provides exposure to global clinical operations, regulatory processes, and opportunities to build expertise in study startup and compliance within a
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Clinical Site Activation Specialist (6-Month Contract) employer: Parexel International
At Parexel, we pride ourselves on being an exceptional employer, offering a collaborative and inclusive work environment where your expertise is highly valued. As a Senior Statistical Programmer, you'll have the opportunity to work on groundbreaking projects while enjoying professional growth, flexible working hours, and a strong commitment to work-life balance. Join us in the UK, Poland, Serbia, or Hungary, and unlock your full potential with our dedication to employee development and quality management.
