Principal Clinical Evidence Specialist - Pain Intervention - Fridley, MN (Onsite)

About the position

At Medtronic, you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. Medtronic is at the forefront of innovation in pain management, offering advanced, evidence-based therapies for patients suffering from chronic and severe pain. Through a comprehensive portfolio of neurostimulation and targeted drug delivery solutions, Medtronic empowers healthcare professionals to personalize treatment and help patients regain control over their lives. These minimally invasive therapies are designed to reduce pain, improve function, and enhance overall quality of life, particularly for individuals who have not found relief through conventional treatments. With a strong commitment to clinical excellence and ongoing support, Medtronic partners with medical professionals to deliver proven outcomes in the evolving field of pain care. Join a diverse team of innovators who bring their worldview, their unique backgrounds and their individual life experiences to work every day. It's no accident - we work hard to cultivate a workforce that reflects our patients and partners. We believe it's the only way to drive healthcare forward and remain a global leader in medical technology and solutions.

Responsibilities

• Leads the creation and implementation of publication and evidence dissemination strategies, including writing manuscripts, abstracts, posters, and presentations based on internal clinical research.
• Collaborates with external physicians and healthcare professionals to co-author content and enhance the visibility of clinical evidence.
• Maintains a well-organized repository of internal publications and relevant peer-reviewed literature.
• Contributes to the development of key clinical documents such as Clinical Investigation Plans (CIPs), IDE submissions, and publication plans.
• Supports investigator meetings, advisory boards, and publication committees to guide evidence generation and strategy.
• Provides clinical input for Corrective and Preventive Actions (CAPAs) and Field Clinical Actions (FCAs).
• Ensures claims matrices are current and compliant with clinical evidence and regulatory standards.
• Drafts and edits scientific reports, comprehensive reviews, and materials for internal and regulatory use.
• Prepares responses to audit and regulatory queries and ensures readiness for compliance inspections.
• Offers clinical expertise across cross-functional teams including marketing, health economics, R&D, reimbursement, and regulatory affairs.
• Conducts clinical reviews of marketing materials to ensure scientific accuracy and compliance.
• Leads or contributes to gap analyses, evidence strategy development, and the creation of medical evidence reports.
• Assesses external research proposals for scientific rigor and oversees deliverables to ensure milestone-based compliance.
• Represents the clinical function on cross-functional teams and in external business collaborations.
• Communicates effectively with senior internal stakeholders, external partners, and vendors to align on strategic goals.
• Ensures all work aligns with FDA/ISO regulations, Medtronic policies, and quality system requirements.

Requirements

• Bachelor's degree with at least 7 years of clinical research experience in studies, publications, and/or program management.
• OR an advanced degree with at least 5 years of experience in studies, publications, or program management.

Nice-to-haves

• Experience in technical writing including clinical study plans, clinical reports, scientific manuscripts, clinical evidence reports.
• Proven record in leading study publications including authorship.
• Demonstrated ability in working within a matrix of cross functional stakeholders including project management skills and experience with related tools.
• Familiarity with ICMJE guidelines and Good Publication Practices Knowledge in the areas of neurology and/or psychiatry.
• Understanding of clinical research study design, Good Clinical Practices, and global clinical regulations (e.g., FDA, ICH guidelines) for medical devices, biologics, and/or pharmaceuticals.
• Demonstrated ability to identify and adapt to shifting priorities and competing demands, and maintain composure in difficult circumstances.
• Ability to provide performance feedback and to appropriately respond to feedback from customers and coworkers.
• Willingness to accept challenging assignments and engage in professional developmental activities.
• Strong analytical and critical thinking skills with the ability to identify and resolve issues efficiently.

Benefits

• Health, Dental and vision insurance
• Health Savings Account
• Healthcare Flexible Spending Account
• Life insurance
• Long-term disability leave
• Dependent daycare spending account
• Tuition assistance/reimbursement
• Simple Steps (global well-being program)
• Incentive plans
• 401(k) plan plus employer contribution and match
• Short-term disability
• Paid time off
• Paid holidays
• Employee Stock Purchase Plan
• Employee Assistance Program
• Non-qualified Retirement Plan Supplement (subject to IRS earning minimums)
• Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums)