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

Eagleston Financial Group; United Kingdom; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading technology company in the United Kingdom is seeking a Lead for Evidence Analysis, Evaluation, and Communications. In this role, you will lead initiatives in translating clinical evidence into strategic impact, managing the development of Clinical Evaluation Reports, and collaborating on regulatory submissions. Ideal candidates will possess strong scientific writing and project management skills, a degree in a biomedical discipline, and at least 5 years of experience in the medical device or pharmaceutical sectors. This position offers generous benefits and a hybrid working model.

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 regulatory documents aligned with EU MDR.

Responsibilities

• Lead the development of Clinical Evaluation Reports (CERs).
• Conduct systematic literature reviews for regulatory submissions.
• Act as subject matter expert during audits and regulatory reviews.

Skills

Literature reviews

Clinical data analysis

Regulatory document authoring

Scientific writing

Project management

Education

Degree in biomedical sciences or clinical discipline

PhD (preferred)

Job description

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

Life. Unlimited. At Smith+Neu 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).

Additional Information

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.

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.

Your Wellbeing: Private health and dental plans, healthcare cash plans, income protection, life assurance.

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.

Employment details

Seniority level: Mid‑Senior level

Employment type: Full‑time

Job function: Management

Industries: Strategic Management Services