Community Patient Outreach Specialist
Synapticure Inc.
Clinical Research Program Manager
Medtronic
full-time
Posted on:
Origin: • 🇺🇸 United States • California
Visit company websiteSalary
💰 $144,800 - $217,200 per year
Job Level
Mid-LevelSenior
About the role
- Lead strategic and tactical elements of clinical programs, representing the Clinical function for a specific therapy segment (Peripheral Vascular Health)
- 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
- Provide program-specific guidance to Clinical Research Specialists and Clinical Study Support Coordinators and synthesize updates for Clinical Research and PVH leadership
- Champion clinical programs that align with strategic PVH objectives and take independent initiative to navigate diverse inputs and requirements
- Operate at both strategic and tactical levels with expertise in prospective and retrospective study design and patient-level data
Requirements
- Bachelor's degree
- Minimum of 5 years of clinical research study management experience OR Masters degree with a minimum of 3 years OR PhD with 3 years clinical research study management experience
- Medical Device clinical study design (Nice to Have)
- Clinical research study management (Nice to Have)
- Demonstrated experience leading cross functional teams (Nice to Have)
- Strong expertise in communication, collaboration, and clinical study operations
- Strong understanding of clinical study design, including prospective and retrospective study design
- Appreciation of patient-level data and knowledge of compliance and regulatory requirements
- Ability to coordinate financial, labor, and clinical program deliverables across Clinical Operations and Core Teams
- Provide program-specific guidance to Clinical Research Specialists and Clinical Study Support Coordinators
- Synthesize updates for Clinical Research and PVH leadership
- For patient-facing roles: comply with hospital/clinic credentialing requirements where applicable
- Must be able to work a minimum of 4 days a week onsite (in-person exchanges are invaluable)
- Regular mobility, computer interaction, and communication with peers and co-workers (physical job requirements)
