SRG seeks a Regulatory Consultant to join the Clinical Trial Strategy & Submissions team in Maidenhead. The role focuses on advancing CTAs, EU CTR submissions, and regulatory planning for global programmes.
You will provide regulatory strategies, collaborate across functions, and ensure timely submission and inspection readiness. A 12-month contract supports a robust clinical development portfolio.
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EU CTR CTA Regulatory Lead (On-site Maidenhead, 12M) 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.
