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

SRG; Normanton on Trent; On-site; GBP 70,000 - 100,000; Full time

Job summary

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.

Qualifications

• CTA experience with global submissions to regulators.
• Understanding of EU CTR processes and requirements.
• Experience working in a complex matrix organisation.

Responsibilities

• Manage CTAs and maintain submission documentation lifecycle.
• Provide regulatory advice on strategies and country requirements.
• Act as SME on EU CTR submissions for complex/trial platforms.
• Guide cross-functional teams through EU CTR processes and training.

Skills

CTA experience

Global submissions

Regulatory strategy

Cross-functional collaboration

English fluency

Education

Bachelor’s degree in Life Sciences

Advanced Life Sciences degree

Tools

MS Word

Excel

PowerPoint

Adobe Acrobat

Regulatory databases

Job description

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.