PURPOSE
The Medical Science Liaison supports medical and business strategies for compounds through field-based activities aligned to overall medical goals and objectives. Establishes Takedaโs presence with thought leaders and academic institutions in defined geographies for assigned therapeutic areas.
Key responsibilities
- Provide medical insights, intelligence, and recommendations from the field to support development and life-cycle management of Takeda compounds.
- Offer medical and scientific expertise to commercial partners as needed within regulatory guidelines.
- Compliantly connect customers to Takeda to advance medical strategy and improve patient outcomes.
Key job accountabilities (minimum 80% externally focused KOL/HCP activities)
- Build and maintain professional relationships with KOLs/HCPs per territory plans developed by the Field Medical Lead.
- Demonstrate advanced knowledge of assigned disease areas/products and the therapeutic area competitor landscape.
- Analyze and interpret complex scientific information and disseminate it to KOLs/HCPs in a compliant, fair-balanced, non-misleading manner.
- Support strategically aligned Takeda-sponsored research; assist with facilitation of medical collaborative studies and investigator-initiated research.
- Collect, interpret, and internally communicate medical insights from KOLs/HCPs to inform/refine medical strategies and tactics.
- Execute field-based medical education programs; support advisory boards as needed.
- Identify and facilitate partnership opportunities between KOLs/HCPs and Takeda.
- Participate in executing medical strategy at medical conferences (e.g., booth activities, interactions with KOLs/HCPs, cover key sessions, internal communication of insights).
- Compliantly address unsolicited requests for medical information from HCPs and related stakeholders.
- Ensure MSL metrics (quantitative and qualitative) are achieved.
- Complete required customer activity documentation (e.g., CRM entries/insights capture), training, expense reporting, and administrative responsibilities in a timely, accurate, compliant manner.
- Assist with clinical education, publications, communications, training, and advisory programs.
- Assist in identifying/evaluating/screening qualified research sites; support clinical trial sites per the Enterprise Engagement Model.
- Provide subject matter expertise and clinical/scientific education for cross-functional partners.
- Perform all company business in full compliance with applicable regulations (e.g., IMC, PAAB), policies/procedures, and industry/legal requirements.
Competencies (skills/knowledge)
Occupational knowledge and skills
- Solid scientific background; ability to think strategically and critically.
- Therapeutic area knowledge (prior experience preferred).
- Ability to communicate using highly technical/scientific language with thought leaders and internal/external stakeholders.
- Firm understanding of pre-clinical and clinical drug development phases/processes/techniques.
- Understanding of Canadian healthcare infrastructure and relevant legislation/codes/guidelines; competitor activities; market dynamics.
- Strong business acumen.
- Self-motivated and self-directed; proven teamwork, leadership, timely decision-making, and results orientation.
- Excellent oral/written communication and interpersonal skills.
- Ability to influence without authority and build relationships with decision-makers.
- Excellent presentation skills.
Digital competencies
- Collect/analyze/interpret data to inform decisions and drive outcomes.
- Work effectively in virtual/remote settings using digital collaboration tools (e.g., MS Teams).
- Leverage digital tools/platforms/AI and Microsoft Office to communicate and perform tasks efficiently.
- Understand cybersecurity threats and best practices to protect sensitive information/systems.
Education, licenses/certifications, experience
- Advanced degree required (MD, PharmD, or PhD); years of experience may be considered depending on relevant pharmaceutical industry experience and/or clinical work/research/academic endeavors.
- Minimum 5 years of experience in pharmaceutical industry and/or relevant clinical experience (or equivalent combination).
- Therapeutic area experience is an asset.
- Bilingual (English/French) preferred.
Travel requirements
- Field-based position; travel to meetings/client sites including overnight trips; some international travel may be required.
Location
- CAN โ Remote (Ontario).
Benefits (Canada-based employees; eligibility varies)
- Short-term and/or long-term incentives; fitness/internet subsidies.
- Medical/dental/vision insurance; basic life and AD&D insurance.
- RRSP participation; company match into DPSP (if eligible).
- Short-term and long-term disability coverage.
- Annual vacation entitlement; additional paid time off and company holidays.
- Tuition reimbursement program.
- Well-being benefits.
Application instructions (as stated)
- By clicking the โApplyโ button, confirm understanding of the application process and that submitted information will be processed per Takedaโs Privacy Notice and Terms of Use.