Strategic Clinical Research Program Manager/Clinical Scientist - PH - Rice Creek, MN (Onsite)

Job description

We anticipate the application window for this opening will close on - 31 Oct 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 LifeThe Neuromodulation and Pelvic Health business develops therapies that address chronic pain, bladder and bowel control disorders, and other conditions that significantly impact quality of life. This team generates the clinical evidence needed to support therapy innovation, regulatory strategies, market access, and physician adoption. Working across Clinical Research, Research & Development, Regulatory, Health Economics and Outcomes Research, Medical Affairs, and Marketing, the function translates business priorities into evidence strategies that drive product and therapy success throughout the lifecycle. This position is based onsite at the Rice Creek East location. Limited travel may be required to support business priorities, stakeholder meetings, and scientific engagements. The Strategic Clinical Program Manager/Clinical Scientist develops and executes integrated clinical evidence strategies that support therapy development, commercialization, and market adoption. This role partners with cross-functional stakeholders to build evidence roadmaps, leverage real-world evidence and emerging analytical approaches, and guide clinical strategy from concept through post-market activities. Primary Responsibilities Strategic Leadership & Evidence Planning Translate business and therapy strategies into clinical evidence generation plans Own the development and lifecycle of integrated evidence roadmaps Drive upstream and downstream alignment with R&D, Regulatory, HEOR, Marketing, and Clinical Affairs AI & RWE Innovation Identify and apply real-world datasets (EMR, claims, registries) and AI/ML tools to enhance clinical strategy Collaborate with Data Science to explore digital biomarkers and AI-enabled clinical insights Guide integration of digital health tools into study design or strategy Execution & Program Oversight Support cross-functional core teams with clinical strategy expertise from concept to post-market Monitor progress, resolve risks, and adapt plans based on closed study insights and market feedback Review and prioritize External Research Program (ERP) and Collaborative Research Studies Stakeholder Engagement Partner with key opinion leaders and scientific advisors to validate strategy direction Collaborate with Medical Affairs and publication teams to drive timely, impactful dissemination Ensure regional evidence needs are captured and incorporated into global strategy Required Qualifications Bachelor's degree with 5+ years of experience in clinical research, clinical strategy, program management, or related healthcare disciplines OR advanced degree with 3+ years of experience in the same areas. 3+ years of experience leading programs, major workstreams, or cross-functional teams. Experience in a healthcare environment, medical device industry, or regulated clinical research setting. Experience developing or executing clinical evidence generation strategies and programs. Experience collaborating across multiple functions to achieve business and clinical objectives. Preferred Qualifications Master's degree (MS, MPH, MBA) or PhD in Life Sciences, Engineering, Public Health, or a related scientific discipline. Knowledge of neuromodulation, pelvic health, pain management, neuroscience, or related therapy areas. Experience with real-world evidence, artificial intelligence, machine learning, or digital health technologies. Experience supporting reimbursement, health economics, market access, or commercialization evidence strategies. Project Management Professional (PMP) certification or formal program/project management training. For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. U.S. Work Authorization & Sponsorship At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment. ‌ Recruitment Fraud Alert We are aware of phishing scams targeting job seekers. Please keep the following in mind: Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com. ‌ Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Salary ranges for U.S (excl. PR) locations (USD):$132,800.00 - $199,200.00 ‌ This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others). The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assis