Lead, Evidence Analysis, Evaluation & Communications (EAEC) - ENT

Smith & Nephew; York and North Yorkshire; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading medical technology company in the UK is seeking an experienced professional to lead cross-functional initiatives in evidence analysis and regulatory evaluation. Responsibilities include developing Clinical Evaluation Reports and collaborating with teams to ensure compliance with global standards. The ideal candidate has at least 5 years of experience in the medical device or pharmaceutical sectors, with a degree in biomedical sciences. The role offers a hybrid working model and generous employee benefits.

Benefits

Generous annual bonus

Flexible vacation

Private health and dental plans

Discounts on gyms and fitness clubs

Qualifications

• Minimum of 5 years’ commercial experience in medical device or pharmaceutical sectors.
• Proven ability to conduct literature reviews and analyze clinical and scientific 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.

Skills

Evidence analysis

Regulatory evaluation

Scientific communication

Project management

Data analysis

Strategic thinking

Education

Degree in biomedical sciences or clinical discipline (PhD preferred)

Job description

Life. Unlimited. At Smith+Naphew we design and manufacture technology that takes the limits off living.

Are you passionate about translating clinical evidence into strategic impact? Join us in a pivotal role where your expertise in evidence analysis, regulatory evaluation, and scientific communication will shape the future of ENT technologies. This is your opportunity to lead cross‑functional initiatives that drive innovation, compliance, and market success.

What will you be doing?

• Lead the development of Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), and Summary of Safety and Clinical Performance (SSCPs) in compliance with EU MDR and global standards
• Conduct systematic literature reviews and data extraction to support clinical evaluations and regulatory submissions
• Act as subject matter expert during audits and regulatory reviews, providing strategic input and supporting new product development decisions
• Perform critical appraisal and synthesis of clinical and scientific data to support product claims and strategic decision-making
• Manage product claims and ensure alignment with clinical evidence and regulatory standards
• Translate complex data into accessible formats such as infographics, summaries, and training materials
• Develop and lead evidence communication strategies for priority brands
• Collaborate with internal teams and external partners to ensure alignment with business strategy and regulatory requirements

What will you need to be successful?

• Minimum of 5 years’ commercial experience in medical device or pharmaceutical sectors, or 8 years combined academic and industry experience
• Proven ability to conduct literature reviews and analyze clinical and scientific data
• Expertise in authoring regulatory documents aligned with EU MDR and related frameworks
• Experience developing promotional and educational materials aligned with clinical evidence and strategy
• Strong scientific writing, data analysis, and project management skills
• Degree in biomedical sciences or clinical discipline (PhD preferred)

You. Unlimited.

• We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.
• Inclusion and Belonging: Committed to welcoming, celebrating and thriving on inclusion and belonging. Learn more about our Employee Inclusion Groups on our website www.smith-nephew.com
• Your Future: Generous annual bonus and pension schemes, Save As You Earn share options
• Work/Life Balance: Flexible vacation and time off, paid holidays and paid volunteering hours so we can give back to our communities
• Your Wellbeing: Private health and dental plans, healthcare cash plans, income protection, life assurance and much more
• Flexibility: Hybrid working model (for most professional roles)
• Training: Hands‑on, team‑customised, mentorship
• Extra Perks: Discounts on gyms and fitness clubs, salary sacrifice bicycle and car schemes and many other employee discounts

Hybrid role #LI-KK1

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