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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
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Looking for your next career move? Join a top company hiring Senior Regulatory Affairs Manager job near me in Birmingham, West Midlands (County)! This is your chance to work on exciting projects, grow professionally, and enjoy a rewarding career with competitive pay and excellent benefits. Whether you're an experienced professional or looking to take the next step, this role offers the perfect opportunity to enhance your skills and make an impact. Don’t miss out—apply today via Vita CV and take your career to the next level!
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