Global Clinical Evaluation Lead - Hybrid/Remote & EU MDR Expert

Corin; Cirencester; Hybrid; GBP 55,000 - 65,000; Full time

Benefits offered by this job

25 days holiday

Private medical insurance with BUPA

Life assurance – 6x basic salary

Pension scheme 6% to 9.7%

Free annual eye tests

Flu vaccinations

Employee referral program £1,000

Job summary

Corin is recruiting a Global Clinical Evaluation Lead to oversee the development and maintenance of clinical evaluation documents across a global medical device portfolio. The role supports EU MDR compliance, global market access, and post‑market surveillance with collaboration across Product Core Teams, regulatory partners, and notified bodies.

You will drive CEPs, CERs, PMCF plans and PMCF reports, and literature activities while coordinating internal and external stakeholders across EU, USA,

Qualifications

• Advanced scientific degree or equivalent
• Minimum 3 years’ industry experience in Medical Devices or Pharmaceuticals
• Proven ability to analyse and summarise clinical data
• Strong understanding of European MDR and regulatory requirements
• Experience with literature searches and critical appraisals
• Excellent written and verbal communication skills

Responsibilities

• Lead the preparation and finalisation of clinical evaluations and documentation per EU MDR
• Coordinate with external evaluation partners and governance meetings
• Prepare responses to review questions from Notified Bodies for product submissions
• Review MDR deliverables including CEPs, CERs, PMCF plans/reports, SSCP
• Contribute to PMCF planning and post-market surveillance across markets
• Represent clinical input in PMS and regulatory discussions with internal teams

Skills

Regulatory knowledge

Communication skills

Project management

Attention to detail

Problem-solving

Stakeholder management

Education

PhD / MSc / MD / BS/BA in sciences or nursing

Job description

Corin is recruiting a Global Clinical Evaluation Lead to oversee the development and maintenance of clinical evaluation documents across a global medical device portfolio. The role supports EU MDR compliance, global market access, and post‑market surveillance with collaboration across Product Core Teams, regulatory partners, and notified bodies.

You will drive CEPs, CERs, PMCF plans and PMCF reports, and literature activities while coordinating internal and external stakeholders across EU, USA,