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Smith+Nephew

Senior Specialist, Evidence Evaluation

Cannock Chase
Posted about 12 hours ago
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Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.

Are you passionate about turning clinical evidence into meaningful impact? This is an opportunity to play a critical role in ensuring innovative medical devices continue to meet the highest standards of safety, performance and regulatory compliance. As a Senior Specialist in Evidence Evaluation, you will work at the heart of clinical and regulatory decision making, shaping how our products are supported, sustained and brought to market across Europe and beyond.

What will you be doing?

In this role, you will bring together scientific expertise, medical writing and regulatory understanding to create robust clinical evidence documentation that underpins the continued CE registration of Smith+Nephew products. You will immerse yourself in clinical data, literature and post market insights, translating complex information into clear, high quality documentation that demonstrates product safety and performance. Working closely with cross functional partners, you will act as a trusted subject matter expert, supporting audits, submissions and strategic business decisions that determine whether products can be placed on the market and how they evolve over time.

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I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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What will you need to be successful?

Success in this role comes from combining technical depth with clarity of thinking and collaboration. You will bring:

  • Strong experience in medical or scientific writing, with the ability to critically appraise and synthesise clinical evidence in line with EU MDR and other related guidance
  • A solid understanding of clinical evaluation processes, literature review methodologies and benefit risk assessment within medical devices or a closely related regulated environment
  • The confidence to act as a subject matter expert, engaging with cross functional teams and supporting regulatory interactions, audits and submissions
  • A proactive and organised approach, with the ability to manage complex documentation, deadlines and priorities independently while working as part of a collaborative team

You. Unlimited.

We believe in creating the greatest good for society. Our Strongest investments are in our people and 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)

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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
  • Many other Employee discounts

Stay connected by joining our Talent Community.

We're more than just a company - we're a community! Follow us on LinkedIn to see how we support and empower our employees and patients every day.

Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You. Unlimited., life, culture, and benefits at S+N.

Explore our website and learn more about our mission, our team, and the opportunities we offer.

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Skills

Medical writing
Scientific writing
Clinical evidence appraisal
EU MDR compliance
Clinical evaluation processes
Literature review methodologies
Benefit risk assessment
Regulatory compliance
Post market insights
Cross functional collaboration
Audit support
Regulatory submissions

Location

Cannock Chase, England, United Kingdom

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