Regeneron UK Limited is seeking a Clinical Study Associate, Clinical Operations to support multiple trials from our Hybrid Uxbridge office. The role involves ensuring compliance with SOPs, GCP, ICH guidelines, and regulations, plus coordinating study team meetings and essential document workflows.
The ideal candidate has 0-1 year of relevant experience, a life sciences degree, and familiarity with CTMS/eTMF systems to maintain accurate trial data and regulatory submissions.
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Clinical Trials Coordinator – Hybrid UK in Uxbridge employer: Regeneron UK Limited
Regeneron UK Limited is an exceptional employer, offering a dynamic and collaborative work culture in Uxbridge that fosters innovation and professional growth. With a strong emphasis on employee development, you will have the opportunity to lead impactful projects in Global Patient Safety while working alongside talented cross-functional teams. The company's commitment to science-driven excellence and patient safety makes it a rewarding place for those looking to make a meaningful difference in the field of rare diseases.
