Senior Clinical PD Program Manager - PH - Fridley, MN (Onsite)
Job
Medtronic
Fridley, MN (In Person)
$223,000 Salary, Full-Time
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Job Description
Senior Clinical PD Program Manager
- PH•Fridley, MN (Onsite) Medtronic•3.
- $267,600 a year 19 hours ago Benefits Health savings account Employee stock purchase plan Paid holidays Disability insurance Dental insurance 401(k) Flexible spending account Tuition reimbursement Paid time off Employee assistance program Vision insurance 401(k) matching Life insurance Paid sick time Qualifications Developing medical devices Master's degree in business administration Stakeholder engagement Master's degree in business Clinical program implementation Budget control New product development 5 years Clinical trial projects Team development Clinical research compliance Bachelor's degree Continuous improvement Decision making Mentoring UX Software development Scope management Design for manufacturability (DFM) Regulatory submissions Budget management in healthcare Manufacturing Financial management Senior level Cross-functional collaboration Medical affairs Master of Business Administration Project leadership Cross-functional team management Leadership Full Job Description We anticipate the application window for this opening will close on•23 May 2026 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all.
LinkedIn:
Medtronic Pelvic Health 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. Responsibilities may include the following and other duties may be assigned . Lead cross-functional teams to align objectives, deliverables, decisions, and milestone timelines. Own program scope, schedule, budget, and resources while proactively managing risks, dependencies, and financial performance. Drive day-to-day execution to deliver programs on time, within scope, and on budget; escalate issues with clear recommendations. Partner with global cross-functional teams to ensure solutions meet business needs and regulatory requirements. Integrate pre- and post-market clinical strategies and evidence-generation plans into program execution in collaboration with Clinical Research and Medical Affairs.
Location :
Rice Creek East/Fridley, MN (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 25% of domestic or international travel to enhance collaboration and ensure successful completion of projects. Must Have (Minimum Requirements) To be considered for this role, please ensure the minimum requirements are evident on your resume . Bachelor's degree in technical discipline with minimum of 7 years of relevant experience, OR Advance degree in technical discipline with minimum of 5 years of relevant experience. Nice to Have (Preferred Qualifications) Advanced degree or MBA strongly preferred. 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 (e.g., design changes/DRM), 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.
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. Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued. 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):$178,400.00- $267,600.
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