Senior Regulatory Affairs Manager

Senior Regulatory Affairs Manager (Remote - EU/UK)

​Are you a regulatory expert with a passion for oncology clinical trials? Join a global CRO with over 40 years of experience in advancing cancer research.

We’re looking for a Senior Regulatory Affairs Manager to lead and support regulatory activities across Europe. This fully remote role is open to candidates based in the UK, France, Italy, Spain, Sweden, or Ireland.

​What You’ll Do:

• Lead CTA submissions and regulatory strategies across EU/UK

• Serve as the regulatory liaison for multi-continental oncology trials

• Collaborate cross-functionally with Clinical Ops, Medical Writing, QA, and more

• Stay ahead of evolving EU/UK regulations and provide expert guidance

What You’ll Bring:

• 5+ years in regulatory affairs within clinical trials (CRO experience preferred)

• Hands-on experience with CTIS and IRAS CTA preparations and submissions

• Strong knowledge of ICH-GCP and EU/UK regulatory frameworks

• Excellent communication, organization, and problem-solving skills

• Fluent English required

Ready to make a difference in cancer research? Apply now and help shape the future of oncology trials.