We anticipate the application window for this opening will close on - 3 Oct 2025
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.
A Day in the Life Peripheral Vascular Health therapies treat patients with Peripheral and Carotid Artery Disease, End-Stage Renal Disease, Superficial and Deep Venous Diseases, and a variety of conditions treated with Peripheral Embolization. The operating unit leads the way in the Superficial Venous, Deep Venous Stenting, and Drug-Coated Balloon markets, caring for nearly 1 million patients globally with lifesaving and life-enhancing therapies.
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We're working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.
This position will be based in Plymouth, MN or Santa Rosa, CA.
The Clinical Program Manager (CPM) for Peripheral Vascular Health (PVH) serves as a critical liaison between the Clinical Research department and cross-functional teams within a specific therapy segment. This role requires strong expertise in communication, collaboration, and clinical study operations.
From a communication standpoint, the CPM must demonstrate a customer-centric approach while navigating both the Medtronic matrix and external healthcare providers. Key communication responsibilities include coordinating financial, labor, and clinical program deliverables across Clinical Operations and Core Teams, providing program-specific guidance to Clinical Research Specialists and Clinical Study Support Coordinators, and synthesizing updates for Clinical Research and PVH leadership.
Collaboration is essential, as the CPM champions clinical programs that align with strategic PVH objectives. This involves fostering productive stakeholder relationships and taking independent initiative to navigate the diverse inputs, requirements, and perspectives inherent in complex clinical programs.
Additionally, the CPM must possess a strong understanding of clinical study design to operate effectively at both strategic and tactical levels. This includes expertise in prospective and retrospective study design, an appreciation of patient-level data, and a thorough knowledge of compliance and regulatory requirements.
Responsibilities may include the following and other duties may be assigned:
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