We anticipate the application window for this opening will close on - 30 Jun 2026

 

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life

Across our global Neuroscience organization, we advance care for some of medicine’s most complex neurological and spinal conditions. By combining innovative technology, data-driven insights, and deep clinical expertise, we partner with physicians and health systems to improve how patients are treated and supported throughout their care journey.

         

         

Our Neuromodulation operating unit delivers advanced therapies for chronic pain, movement disorders, and nervous system conditions, offering SCS, DBS, and targeted drug delivery. Through proven technology, clinical evidence, and innovation, we provide personalized solutions that restore function and enhance quality of life. 

Check us out on LinkedIn: Medtronic Brain Modulation and Pain Interventions

As Senior Clinical Evidence Specialist (CES), you will plays a key role within the Pain Interventions evidence team. This role involves literature review, medical evidence gap analysis, publication planning, writing manuscripts, facilitating publication committees, reviewing marketing materials, providing SME for Clinical Evaluation Reports (CERs) and evaluating physician-sponsored studies. Additionally, the CES will collaborate with cross-functional teams, including marketing, medical affairs, reimbursement, research, and study teams, and may serve as a clinical representative on core teams.

Responsibilities may include the following and other duties may be assigned.

• Create and submit manuscripts based on clinical studies and/or scientific reports.

• Create and submit abstracts, poster presentations, podium presentations.

• Engagement with external physicians/HCP(s) on publications, scientific communications and evidence dissemination.

• Conduct Literature reviews, summarize scientific findings, develop medical evidence reports, and lead cross-functional evidence gap-analysis.

• Contribute to publication planning and evidence strategy development.

• Support study Investigator meetings and/or Advisory Boards.

• Maintain a database of peer-reviewed literature and internal publications.

• Create responses for audit/submission queries.

• Reports instances of complaints/adverse events from literature to Global Clinical Health (GCH).

Location: Rice Creek/Fridley (Onsite)

Onsite:

At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. We’re working onsite 4 days a week to drive performance, foster an environment of belonging, and collaborate to inspire as we engineer the extraordinary. This role will require 10% of travel to enhance collaboration and ensure successful completion of projects.

A Day in the Life

• Write and edit manuscripts, comprehensive reviews, and scientific reports for regulatory submissions and internal use.

• Provide clinical expertise and collaborate with cross-functional teams, including marketing, health economics, reimbursement, research & development, and regulatory affairs.

• Conduct clinical review of marketing materials

• May facilitate Publication Committees and Plans in collaboration with Physician Investigators to ensure accurate high impact publications. May work internally to obtain input on Publication Plans with updates regularly to address evidence gaps. 

• May work with investigators to resolve problems quickly and effectively.

• May serve on cross-functional core teams as the clinical representative

• May work on business collaborations with external partners

• May develop medical evidence reports, lead cross-functional gap analysis, and propose future strategy.

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