Manager, Medical Affairs T2D and Data Products Franchise (Hybrid)

About the Role

Key Responsibilities

• Provide effective medical leadership and collaborate within project teams to advise and guide strategic objectives and operational decisions impacting global project direction.
• Act as the medical expert, utilizing knowledge of diabetes management, standards of care, published data, and key opinion leader insights.
• Shape medically sound product design requirements, assess system and user error risks, and advise on risk control measures for safe and effective use.
• Engage with clinical validation teams to formulate study needs, evaluate outcomes, and confirm risk control effectiveness.
• Develop evidence generation strategies to support regulatory approval and product claims based on program objectives and cross-functional inputs.
• Translate data into meaningful insights supporting regulatory requirements, commercial claims, and product messaging.
• Gather and translate medical intelligence from industry experts by engaging with Medical Science Liaison team, investigators, and advisory boards.
• Develop and prepare medical go-to-market strategies and content for regional teams, including professional education, conference presentations, and healthcare provider engagements.
• Establish professional learning needs and define educational requirements to ensure safe and effective use of Omnipod and related products.

Requirements

• Minimum of 5+ years in clinical, industry, or research settings related to diabetes and devices such as insulin pumps or continuous glucose monitors.
• Life science degree with 5+ years of experience in medical affairs or medical strategy within medical device or pharmaceutical industry.
• Proven experience in developing and leading medical strategy implementation.
• In-depth understanding of diabetes (type 1 and type 2), disease pathophysiology, treatment options, risks, and outcomes.
• Advanced knowledge of diabetes technology, including automated insulin delivery systems.
• Experience designing research studies and interpreting data.
• Skilled in medical communication to diverse audiences.
• Strong technical and business acumen, with understanding of US and global regulatory environments for medical devices.
• Ability to thrive in a fast-paced, multitasking environment and effectively prioritize projects.
• Working knowledge of relevant software programs such as Microsoft Office Suite, Adobe Products, and medical communication tools.

Nice to Have

• Advanced degree and/or healthcare-related certification (e.g., PA/NP, Registered Nurse, Registered Dietitian, Certified Diabetes Care and Education Specialist, PhD, PharmD).

Qualifications

• 5+ years of experience in clinical, industry, or research settings related to diabetes and medical devices.
• Life science degree or equivalent experience in medical affairs or medical strategy.

Benefits & Perks

• US base salary range of $131,400.00 - $197,100.00, determined by role, level, and location.
• Potential for bonus, equity, and benefits (not specified in detail).
• Hybrid work environment requiring on-site presence at least 3x/week with remote work possible on other days.
• Travel within North America and internationally up to 15% of the time.