EU CTR Regulatory Lead — Clinical Trial Submissions

SRG is seeking an experienced Regulatory Consultant to join our Clinical Trial Strategy & Submissions team in Maidenhead. Responsibilities include managing CTAs, amendments and end-of-trial notifications to support global clinical development.

On-site 3 days a week (Tue–Thu). The role requires 5–6+ years CTA experience, strong EU CTR knowledge, cross-functional collaboration, and excellent written and verbal English.

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