At a Glance
- Tasks: Support clinical studies from start to finish, ensuring everything runs smoothly.
- Company: Join Regeneron Pharmaceuticals, a leader in innovative healthcare solutions.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic team environment with a focus on collaboration and innovation.
- Why this job: Make a real difference in clinical research and patient care.
- Qualifications: 2 years of relevant experience and knowledge of ICH/GCP preferred.
The predicted salary is between 35000 - 45000 £ per year.
Regeneron Pharmaceuticals, Inc. is seeking a Clinical Study Specialist to join our Clinical Trial Management team.
You will provide technical and administrative support to study teams from site activation through close-out, ensuring studies stay on track.
In this role you will coordinate data, prepare documents, and maintain TMF reconciliations while partnering with Clinical Study Leads, CROs, and study sites.
A minimum of 2 years' relevant experience and knowledge of ICH/GCP is preferred.
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Clinical Trial Operations Specialist in Cambourne employer: Regeneron Pharmaceuticals, Inc
At Regeneron, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work culture that fosters innovation and collaboration. As a Senior Manager in our Global Development Quality Assurance team, you will have the opportunity to lead impactful audit strategies while working remotely from the UK or Ireland, benefiting from a comprehensive rewards package that includes competitive bonuses, health and wellness programs, and robust employee growth opportunities. Join us in making a meaningful difference in patients' lives while enjoying a supportive environment that values diversity and professional development.
Contact Details:
Regeneron Pharmaceuticals, Inc Recruitment Team
