About the role:

The Medical Affairs Manager (MAM) will play a key role in supporting and executing the global medical strategy. This individual will drive medical education, therapy adoption, and strategic initiatives that elevate clinical understanding and real-world impact. The MAM will serve as a critical liaison between internal teams and healthcare professionals (HCPs), amplifying clinical data, promoting appropriate therapy use, and delivering insights to shape ongoing innovation.

This role also brings medical and scientific expertise to cross-functional teams, supporting the alignment and delivery of Medical Affairs objectives in support of the overall Cryoablation strategy.

Responsibilities will include:

• Deliver on the Global Medical Plan by supporting data generation, knowledge exchange, education, and scientific initiatives related to Cryoablation.
• Collaborate with Medical, Clinical, and Health Economics & Market Access teams to align evidence planning and execution.
• Analyze and interpret new clinical publications and competitive trial data, support dissemination strategies.
• Develop the clinical evidence story and oversee implementation through the field medical team.
• Create scientific content and medical materials to support external education and internal enablement.
• Provide medical expertise to Commercial, Regulatory, and Market Access teams; review promotional materials for accuracy and compliance.
• Lead strategic planning of symposia and sponsored educational events at global and regional conferences.
• Support Medical Education by aligning therapy objectives and preparing faculty for company-sponsored events.
• Identify and build relationships with key opinion leaders (KOLs), expert speakers, and academic leaders to support educational and data dissemination initiatives.
• Communicate complex clinical data clearly to physicians and internal stakeholders; demonstrate deep understanding of trial design, data interpretation, and real-world application.
• Ensure KOLs and podium speakers have access to the latest clinical data and pipeline updates.
• Uphold compliance standards for all physician interactions and programs in accordance with company policies and regulatory guidelines.

Qualifications:

Required qualifications:

• Advanced degree, ideally a postgraduate qualification or equivalent experience in healthcare practice or research.
• Minimum of 5 years of experience in a medical or clinical role within the industry.
• Therapeutic area experience in oncology.
• Proven experience interpreting and communicating clinical data to both internal stakeholders and physicians.
• Strong relationship-building skills, particularly with healthcare professionals in the field.
• Solid understanding of regulatory guidelines and Good Clinical Practices.
• Ability to travel within North America and internationally.

Preferred qualifications:

• Highly motivated and collaborative with the ability to drive cross-functional alignment.
• Strong time management skills with the ability to prioritize multiple initiatives in a fast-paced environment.
• Demonstrated commitment to compliance, patient safety, and product quality.
• Proven ability to work in a matrix environment with global stakeholders.