SRG in Maidenhead seeks an experienced Regulatory CTA specialist to manage a portfolio of CTAs, prepare and maintain submission documentation, and guide cross-functional teams through EU CTR processes.
You will advise on submission strategy, monitor milestones, support inspection readiness, and ensure timely compliance with internal and regulatory requirements in a fast-paced, globally collaborating environment.
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EU CTR Submissions Lead — CTA Contract (On-site) in Maidenhead employer: SRG
As a Senior Clinical Trial Manager at our company, you will thrive in a dynamic and collaborative work environment that prioritises innovation and employee development. We offer competitive benefits, a strong focus on professional growth, and the opportunity to work alongside industry leaders in a location renowned for its commitment to advancing clinical research. Join us to make a meaningful impact in the field of clinical trials while enjoying a supportive culture that values your contributions.
