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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EU CTR Regulatory Lead — Clinical Trial Submissions 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.
