We anticipate the application window for this opening will close on - 26 Sep 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

Join Medtronic’s Neuromodulation and Pelvic Health team as a Strategic Clinical Program Manager, where you’ll shape the clinical evidence strategy that drives therapy innovation, adoption, and access. This is a high-impact, cross-functional role that bridges science, strategy, and execution, developing clinical roadmaps and incorporating AI and real-world evidence (RWE) to transform patient outcomes. 

 

Key Responsibilities 

 

Strategic Leadership & Evidence Planning 

• Translate business and therapy strategies into clinical evidence generation plans 

• Own the development and lifecycle of integrated evidence roadmaps 

• Drive upstream and downstream alignment with R&D, Regulatory, HEOR, Marketing, and Clinical Affairs 

 

AI & RWE Innovation 

• Identify and apply real-world datasets (EMR, claims, registries) and AI/ML tools to enhance clinical strategy 

• Collaborate with Data Science to explore digital biomarkers and AI-enabled clinical insights 

• Guide integration of digital health tools into study design or strategy 

 

Execution & Program Oversight 

• Support cross-functional core teams with clinical strategy expertise from concept to post-market 

• Monitor progress, resolve risks, and adapt plans based on closed study insights and market feedback 

• Review and prioritize External Research Program (ERP) and Collaborative Research Studies  

 

Stakeholder Engagement 

• Partner with key opinion leaders and scientific advisors to validate strategy direction 

• Collaborate with Medical Affairs and publication teams to drive timely, impactful dissemination 

• Ensure regional evidence needs are captured and incorporated into global strategy 

 

 

Must-Have Qualifications 

• Bachelor’s degree and 7+ years of clinical research, strategy, or program management experience 

OR advanced degree with 5+ years of relevant experience 

• 3+ years of leadership experience (e.g., leading programs, workstreams, or cross-functional teams) 

• Experience in a healthcare setting, ideally in medical devices or regulated clinical research 

 

Preferred Qualifications 

• Master’s degree (MS, MPH, MBA) or PhD in life sciences, engineering, or public health 

• Knowledge of neuromodulation, pelvic health, pain, or neuroscience therapy areas 

• Strong familiarity with real-world evidence (RWE), AI/ML applications, or digital health 

• Experience influencing upstream pipeline and downstream reimbursement/market access strategy 

• PMP certification or formal project/program management training 

• Excellent stakeholder communication and scientific writing skills