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Senior Global Clinical Strategy Specialist (Sports Medicine)

extra holidays
Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Extensive experience in clinical strategy roles, Background in medical devices or pharmaceuticals, Strong understanding of evidence generation, Relevant educational qualifications in a related field.

Key responsabilities:

  • Support strategic clinical direction for Sports Medicine portfolio
  • Lead clinical aspects of New Product Development

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Smith+Nephew XLarge http://www.smith-nephew.com/
10001 Employees
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Job description

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

In our pursuit of designing and manufacturing innovative medical devices that transform patient care, we are seeking a Clinical Strategy expert to join our collaborative and trailblazing team, someone who will be instrumental in performing strategic plans and capturing crucial clinical and economic evidence. Your efforts will not only accelerate the global introduction and adoption of new products but also ensure the sustained availability of approved devices, all while adhering to stringent regulatory standards.

In this role, you will collaborate closely with a diverse array of internal and external partners, to drive evidence generation activities.

Your deep understanding of our dedication to clinical evidence collection will empower you to support strategies that identify and address any gaps in our clinical evidence, ensuring we remain at the forefront of medical device innovation.

What will you be doing?

  • Supporting the strategic clinical direction for our Sports Medicine product portfolio.
  • Leading clinical aspects of the New Product Development program through execution of the evidence generation strategies.
  • Design and execute evidence generation activities to support global market adoption and market access initiatives.
  • Work with Key Opinion Leaders to design and activate evidence strategies to support publication submissions and conference presentations.
  • Working closely with other collaborators and relevant clinical strategy leads to support regulatory related activities and submissions.

What does success look like?

Our successful candidate will be highly educated in a relevant subject area, along with extensive working experience in a Clinical, Research & Development, Scientific, Medical affairs or Regulatory role within a Medical Device or Pharmaceutical organisation.

Within your previous roles, you will have gained relevant experience in supporting strategies whilst generating clinical evidence.

You. Unlimited

165 years of groundbreaking innovation requires a steadfast focus on what’s next. We’re passionate about you. You’re what’s next...

  • 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 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.

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Experience

Level of experience: Senior (5-10 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Collaboration
  • Communication
  • Problem Solving

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