Global Clinical and Medical Affairs Manager

Creo Medical; Chepstow; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A medical technology company in the UK is seeking a Global Clinical and Medical Affairs Manager to lead global clinical programs. This pivotal role requires proven experience in clinical trials, regulatory frameworks, and the ability to engage with key opinion leaders. The ideal candidate will have a degree in life sciences, medicine, or a related field, and possess exceptional communication skills. This position offers a chance to shape the clinical foundation of life-saving technologies.

Qualifications

• Proven experience in global clinical or medical affairs within the medtech or life sciences sector.
• Hands-on track with clinical trials, scientific communication, and KOL engagement.
• Strong understanding of global regulatory and clinical frameworks.

Responsibilities

• Lead the planning and execution of global clinical trials.
• Shape clinical evidence strategies for regulatory approvals.
• Collaborate with Regulatory Affairs on clinical submissions.

Skills

Clinical trials management

Scientific communication

Regulatory knowledge (FDA, EMA, ICH-GCP)

KOL engagement

Collaborative leadership

Education

Degree in life sciences, medicine, or related discipline

MSc, PhD, or MD

Job description

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:

• 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.

What You Bring:

• Proven experience in global clinical or medical affairs within the medtech or life sciences sector.
• Hands‑on track 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.

Your Background:

• 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.

Why Join Us?

This is your chance to define the clinical foundation of a category-defining platform — and help ensure the safe, effective global adoption of life‑saving technologies.