EU CTR CTA Regulatory Lead (On-site Maidenhead, 12M)

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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