Global Clinical and Medical Affairs Manager
Creo Medical
Date: 1 day ago
City: Chepstow
Contract type: Full time

Lead the science. Drive the data. Empower safer surgery.
At Creo Medical, we’re on a mission to transform endoscopic surgical care through advanced energy technology. We’re seeking a Global Clinical and Medical Affairs Manager to lead our global clinical programs and shape the medical and scientific foundation of our portfolio. This is a pivotal role at the intersection of clinical research, medical strategy, and market access — perfect for someone who thrives on collaboration, data-driven decision-making, and global impact.
What You’ll Do:
At Creo Medical, we’re on a mission to transform endoscopic surgical care through advanced energy technology. We’re seeking a Global Clinical and Medical Affairs Manager to lead our global clinical programs and shape the medical and scientific foundation of our portfolio. This is a pivotal role at the intersection of clinical research, medical strategy, and market access — perfect for someone who thrives on collaboration, data-driven decision-making, and global impact.
What You’ll Do:
- Lead the planning and execution of global clinical trials across therapeutic areas.
- Shape clinical evidence strategies to support regulatory approvals, product adoption, and market access.
- Own key clinical deliverables — from protocols and safety reporting to publications and HEOR outputs.
- Collaborate with Regulatory Affairs on CERs and clinical sections of submissions.
- Act as a medical affairs leader, engaging with KOLs, clinical advisors, and investigators.
- Represent Creo Medical at advisory boards, scientific meetings, and conferences.
- Provide internal clinical guidance across R&D, product, and commercial teams.
- Proven experience in global clinical or medical affairs within the medtech or life sciences sector.
- Hands-on track record with clinical trials, scientific communication, and KOL engagement.
- Strong understanding of global regulatory and clinical frameworks (FDA, EMA, ICH-GCP).
- Experience in medical monitoring, safety reporting, and evidence generation strategies.
- Exceptional written and verbal communication — capable of making the complex clear.
- Collaborative, proactive, and ready to lead without needing direct reports.
- Degree in life sciences, medicine, or related discipline;
- MSc, PhD, or MD advantageous.
- Based in the UK or USA, with ability to travel internationally as needed. Unrestricted right to work in the UK or USA.
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