Job Description
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.
