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

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

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)