Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.
We believe in our products. We believe that through innovation, development and supporting our customers and patients we can help others achieve a Life Unlimited! Long before any of this is possible, we have to go through many steps that will validate and verify our products, including evidence gathering and evaluation and design verification and validation.
If you thrive in a diverse work environment that champions continuous development and innovation, Smith+Nephew will be the ideal place for you. We are planning for upcoming opportunities which may be perfect for graduates looking to take a first step into a medical writing, clinical studies or clinical study design career path.
Please note – this is an expression of interest and something that we may start recruiting for in the near future.

What will you be doing if you join our Evidence Evaluation team?

• This entry-level clinical and scientific role supports the creation of various reports and plans to back the CE marking of our products. You’ll assist with literature searches, review publications, and help communicate findings. You’ll also locate internal documents to complete sections of these reports and generate related documentation.
• This positon will allow you to gain experience across all three of S+N’s franchises and see firsthand how clinical evaluation reports are created. You’ll support the completion of reports for CE registration, work with Evidence Evaluation Specialists to gather inputs and approvals, and maintain supporting documents and publication databases.
• This role will enhance your understanding of the clinical evaluation process and build your skills in document management and data analysis.
• As an Evidence Evaluation Associate, you’ll help assess device safety and effectiveness, supporting our post-market surveillance and risk management.
• You’ll also assist with documentation for product registration in non-EU countries, giving you insight into global regulatory standards. This position offers a fantastic opportunity to develop your skills and gain experience in a dynamic and impactful field.

What will you need to be successful?
We’re looking for an inquisitive individual with a bachelor’s degree in a relevant biological or clinical field. You should be familiar with performing literature reviews, analysing data sets, and understanding clinical and scientific concepts.
Strong organisational and communication skills are important, as is the ability to work collaboratively.
You. Unlimited

We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.

• Inclusion, Diversity and Equity: Committed to Welcoming, Celebrating and Growing on Diversity, Learn more about our Employee Inclusion Groups on our website
• Your Future: Generous annual bonus and pension Schemes, Save As You Earn share options.
• Work/Life Balance: Flexible Holidays 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.

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• This entry-level clinical and scientific role supports the creation of various reports and plans to back the CE marking of our products. You’ll assist with literature searches, review publications, and help communicate findings. You’ll also locate internal documents to complete sections of these reports and generate related documentation.
• This positon will allow you to gain experience across all three of S+N’s franchises and see firsthand how clinical evaluation reports are created. You’ll support the completion of reports for CE registration, work with Evidence Evaluation Specialists to gather inputs and approvals, and maintain supporting documents and publication databases.
• This role will enhance your understanding of the clinical evaluation process and build your skills in document management and data analysis.
• As an Evidence Evaluation Associate, you’ll help assess device safety and effectiveness, supporting our post-market surveillance and risk management.
• You’ll also assist with documentation for product registration in non-EU countries, giving you insight into global regulatory standards. This position offers a fantastic opportunity to develop your skills and gain experience in a dynamic and impactful field