Ipsen Ltd. is seeking a Clinical Trial Administrator to support Clinical Operations across the study lifecycle, coordinating TMF setup, filing, and study tracking.
You will work with CPMs and TA Directors to ensure regulatory compliance and inspection readiness. Responsibilities include TMF administration, quality checks, archiving, invoice tracking, and data disclosure in line with EFPIA and Sunshine Act requirements; you will also assist with contracts and study documentation, and join study
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Clinical Trial Admin & Study Operations Specialist in Cambridge employer: Ipsen Ltd
Ipsen Ltd is an exceptional employer that prioritises employee growth and well-being, fostering a culture of collaboration and innovation. With a commitment to transforming rare disease care, employees are empowered to make a meaningful impact while enjoying a supportive work environment that values diverse perspectives. Located in the UK, Ipsen offers unique opportunities to engage with NHS organisations and contribute to healthcare transformation, ensuring that every team member can thrive alongside the company's mission to improve patient outcomes.
