Senior Clinical PD Program Manager - PH - Fridley, MN (Onsite)
Not Disclosed•Full-TimeOn-site
location_on4849, 5th Street Northeast, Columbia Heights, Anoka County, Minnesota, 55421, United States
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.
As one of three comprehensive portfolios at Medtronic, Neuroscience is dedicated to improving the lives of people living with neurological disorders, spine conditions, and chronic pain. Guided by our Mission—to alleviate pain, restore health, and extend life—we develop technologies and therapies that help people regain function, reduce pain, and return to the activities that matter most.
Our Pelvic Health operating unit advances care for bladder and bowel control conditions through restorative, minimally invasive neuromodulation therapies. By modulating sacral and peripheral nerves, we deliver personalized, programmable solutions backed by strong clinical evidence to help restore function and improve quality of life.
The Senior Clinical Product Development Program Manager is a cross-functional program leader responsible for driving decision-making and predictable execution within Pelvic Health development programs and clinical studies. You are accountable for the management direction of all phases of design and development of new medical device systems (including software and user experience) and for partnering with Clinical, Regulatory, Quality, and Medical Safety to ensure clinical evidence is scientifically valid, ethically conducted, and aligned to regulatory approvals, reimbursement needs, and therapy adoption.
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 25% of domestic or international travel to enhance collaboration and ensure successful completion of projects.
Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued.
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission unites a global team of 95,000+ passionate people. We are engineers at heart—putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
We anticipate the application window for this opening will close on 23 May 2026.
Work model: On-site
4849, 5th Street Northeast, Columbia Heights, Anoka County, Minnesota, 55421, United States
Columbia Heights, Minnesota
Advanced degree or MBA. Proven experience leading cross-functional teams and programs within a matrixed organization, with responsibility for scope, timelines, budgets, and risk management. Medical device industry experience spanning new product development and sustaining engineering changes, including familiarity with regulatory submissions. Experience incorporating pre- and/or post-market clinical evidence plans into program execution, with working knowledge of GCP and clinical trial compliance requirements. Demonstrated experience managing product indication expansions and global market expansion initiatives. Excellent communication and influencing skills, with the ability to engage effectively across all organizational levels in a global matrix environment. Experience collaborating with manufacturing teams on process characterization, production ramp readiness, and implementation of design or process changes. Strong problem-solving capabilities and risk-based decision-making skills, with a track record of driving meetings toward clear actions and outcomes. Demonstrated cross-functional leadership within a global matrixed environment.
Skills: GCP, Clinical Trial Compliance, Risk Management, Voice Of Customer, Design For Manufacturability, Process Characterization, Regulatory Submissions, Medical Device, New Product Development, Sustaining Engineering Changes.
Education: Bachelor's degree in technical discipline required; Advanced degree in technical discipline preferred; MBA strongly preferred.
