Medtronic is looking to solve healthcare access and equity problems for patients with Peripheral and Carotid Artery Disease, End-Stage Renal Disease, Superficial and Deep Venous Diseases, and other conditions treated with Peripheral Embolization.
Requirements
- Strong expertise in communication, collaboration, and clinical study operations.
- Prospective and retrospective study design expertise.
- Appreciation of patient-level data.
- Thorough knowledge of compliance and regulatory requirements.
- Medical Device clinical study design experience (nice to have).
- Clinical research study management experience (nice to have).
- Demonstrated experience leading cross functional teams (nice to have)
Responsibilities
- Lead strategic and tactical elements of clinical programs, representing the Clinical function for a specific therapy segment.
- Collaborate with cross-functional teams, including Regulatory, Medical Science, Commercial, Healthcare Reimbursement, and Core Teams, to implement clinical programs aligned with Operating Unit objectives.
- Develop and execute compliant, scientifically valid, and efficient clinical programs that inform practice and meet global regulatory standards.
- Foster strong internal and external relationships that embrace customer-centricity and ensure successful clinical program outcomes.
- Provide leadership in conducting clinical studies and supporting regulatory processes to achieve product approval(s).
- Coordinate financial, labor, and clinical program deliverables across Clinical Operations and Core Teams.
- Synthesize updates for Clinical Research and PVH leadership.
Other
- Bachelor's degree or higher.
- Minimum of 5 years of clinical research study management experience (or equivalent with higher degree).
- Ability to work a minimum of 4 days a week onsite.
- Travel requirements not specified.
- Must be able to interact with a computer, and communicate with peers and co-workers.
