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A leading pharmaceutical company is looking for a Medical Affairs executive to provide leadership and strategic oversight in Canada. This role requires a strong background in the pharmaceutical sector, particularly in oncology and neurology, and aims to build a high-performing team while ensuring compliance with regulatory standards. The candidate must exhibit exemplary leadership skills and be capable of influencing decisions at all levels.
Purpose: Leadership and oversight of medical strategy development and execution for the Canadian business across all therapeutic areas. Enterprise leader acting as core member on the Canadian Leadership Team, EUR/INT Regional Medical Leadership Team (EIMALT), reporting to the General Manager, Jazz Pharmaceuticals Canada.
The role is responsible for ensuring all activities are executed in accordance with regulatory and legal frameworks, including but not limited to local Canadian regulations, company policies, healthcare compliance procedures as well as Jazz values
Essential Functions:
Leadership of Medical Affairs Department
Lead, develop, and build a high-performing, fully integrated Medical Affairs Department
Manage, coach, and develop Medical Affairs personnel (direct and indirect reports)
Role model and exemplify Cultural values
Co-lead the development and oversight of the launch center of excellence
Strategic and Tactical Planning
Ensure development and delivery of the Medical Affairs strategy and country plans in close collaboration with business partners, BU heads and General Manager.
Set departmental SMART objectives and track, measure, and report progress of plans and budgets
Ensure Canadian needs are effectively communicated to partners in the EUR/INT regional office to maintain alignment on strategy and plans at all levels
Provide high-quality input in Global/Region TA integrated evidence generation plans and proactively address local-specific evidence gaps with Canadian studies to ensure accelerated access and effective integration of new therapies in routine clinical practice
Build companion data generation strategy to enhance Canadian real-world experience and education
Define early/expanded access programs needs for Canada and support execution of Managed Access Programs (MAPs)
Allocate adequate Medical team capacity to support ongoing R&D program in Canada
Systems, Processes, and Ways of Working
Ensure systems, processes, and ways of working facilitate:
Effective execution of the medical plan
Expert scientific knowledge for all Medical Affairs team members
Effective Key Account Planning with cross-functional partners
Effective planning and utilization of National Key Opinion Leaders
Data generation activities, including Investigator Sponsored Studies
Optimized Canadian participation in priority global registration trials to support development of new innovative therapies, building early advocacy and understanding challenges prior to launch
Digital enablement strategies to optimize stakeholder engagement, education, and insight gathering
Development of ongoing capabilities in the Medical Affairs organization (e.g., strategic account management, diverse stakeholder engagement, AI/digital enablement etc…)
Clinical Research Operations leadership (e.g., for EAPs, IITs, locally-led RWE studies, global studies, etc.)
External Relationships
Develop influential relationships with National Key Opinion Leaders
Attend appropriate scientific congresses to stay abreast of developments and support National KOL activities
Support the development of Jazz EU/RoW positioning as the scientific authority on oncology, helping drive national KOL advocacy through provision of scientific and clinical information via the MSL team
Co-represent Jazz voice and scientific voice together with General Manager
Required Knowledge, Skills, and Abilities:
Strong experience leading medical organizations in Canada with a working knowledge and understanding of the healthcare system
Pharmaceutical industry experience in a comparable role, ideally with knowledge of Oncology, Neurology, and specialty pharma
A proven track record of building high-performing Medical Affairs teams
Must have experience in launching new products, market shaping, and launch readiness activities
Strong leadership skills with demonstrable ability to influence at all levels internally and externally
Ability to drive executional excellence in regulatory, clinical, and medical strategies across a broader regional framework
Understanding of R&D strategy and execution of registration clinical program
Excellent communication skills, including strong presentation skills
Flexible, independent, and proactive working style
Ability to critically analyze complex data
Excellent planning and organizational skills
Strong interpersonal relationship-building skills/collaboration and teamwork
Commitment to advancing Canada’s representation in regional strategic regulatory decisions
Willingness to travel frequently
Bilingual (French and English) is an asset, both spoken and written
Required/Preferred Education and Licenses:
Strong preference for a Medical Doctor or Scientific Graduate (ideally with a higher scientific qualification e.g., PhD or PharmD, etc.)