Lead, Clinical Evidence & Regulatory Communications

Smith & Nephew; Watford; Hybrid; GBP 55,000 - 75,000; Full time

Job summary

A global medical technology company is seeking a Lead for Evidence Analysis, Evaluation & Communications in Watford, UK. The ideal candidate will lead the development of key clinical documents, conduct literature reviews, and manage evidence communication strategies while ensuring compliance with regulatory standards. A degree in biomedical sciences or a related field is essential, along with significant experience in the medical device or pharmaceutical sectors.

Benefits

Generous annual bonus

Pension schemes

Flexible vacation and time off

Private health and dental plans

Discounts on gyms and fitness clubs

Qualifications

• Minimum of 5 years’ experience in medical device or pharmaceutical sectors.
• Proven ability to conduct literature reviews and analyze clinical data.
• Expertise in authoring regulatory documents aligned with EU MDR.

Responsibilities

• Lead the development of Clinical Evaluation Reports and Clinical Evaluation Plans.
• Conduct systematic literature reviews to support clinical evaluations.
• Act as subject matter expert during audits and regulatory reviews.
• Translate complex data into accessible formats for stakeholders.
• Develop evidence communication strategies for priority brands.

Skills

Commercial experience in medical device or pharmaceutical sectors

Conducting literature reviews

Analyzing clinical and scientific data

Authoring regulatory documents

Scientific writing

Project management

Education

Degree in biomedical sciences or clinical discipline (PhD preferred)

Job description

A global medical technology company is seeking a Lead for Evidence Analysis, Evaluation & Communications in Watford, UK. The ideal candidate will lead the development of key clinical documents, conduct literature reviews, and manage evidence communication strategies while ensuring compliance with regulatory standards. A degree in biomedical sciences or a related field is essential, along with significant experience in the medical device or pharmaceutical sectors.