Global Medical Lead, PDT Hematology (f/m/x)
Takeda
August 14, 2026
Remote friendly (Cambridge, MA)
United States
$192,400 - $302,390 USD yearly
Medical Affairs
Position Objectives:
- Lead execution of key Global Medical activities for Prothromplex according to the PDT Benign Hematology GM strategy.
- Define and lead development of global medical launch strategy for Prothromplex and subsequent scientific programs.
- Provide medical and technical support across GPT, R&D, Clinical Science, Quality, Safety, Regulatory, Manufacturing, and Legal.
- Provide medical review to global promotional and non-promotional materials.
- Represent the company with external scientific leaders, patient advocacy groups, and/or regulatory authorities.
- Support strategic partnerships with centers of excellence and KOLs.
Position Accountabilities:
- Lead development/implementation of short- and long-term medical strategies (scientific communication, evidence generation, capability building, KOL engagement).
- Develop global medical plans and pre-/post-launch tactics; manage in-year medical budget and plans.
- Oversee functional plans (publications, medical communications, medical information, medical training).
- Collaborate with business partners to align brand strategy and execution; provide medical affairs/R&D inputs.
- Plan/manage global Advisory Boards; track/manage KOL engagement activities in the KOL platform.
- Support global regulatory meetings; advise on regulatory information (e.g., Package Insert, Patient Information).
- Support clinical research strategy, evidence generation (including Phase IV), and adverse event evaluation.
- Lead capability building with training/continuing education; partner on AI-driven projects.
Required Qualifications:
- Advanced scientific degree (MD preferred; PhD or PharmD).
- 7+ years pharmaceutical experience in Medical Affairs or Clinical Development/R&D or related functions at international level.
- Experience/training in benign hematology and bleeding disorders.
- Medical Affairs experience supporting brands/disease area internationally.
- Experience creating post-approval studies, medical strategies, and launch plans.
- Strong understanding of R&D critical processes and pharmaceutical regulations in key markets.
Additional Information:
- Travel: ~30%.
- Hybrid work.
Compensation/Benefits (as stated):
- U.S. base salary range: $192,400–$302,390.
- Eligible for incentives; medical/dental/vision, 401(k) match, disability, life insurance, tuition reimbursement, paid volunteer time off, holidays, well-being benefits, sick time, and vacation.
Application Instructions:
- Apply via the “Apply” button (application process begins; info processed per Privacy Notice and Terms of Use).
- Lead execution of key Global Medical activities for Prothromplex according to the PDT Benign Hematology GM strategy.
- Define and lead development of global medical launch strategy for Prothromplex and subsequent scientific programs.
- Provide medical and technical support across GPT, R&D, Clinical Science, Quality, Safety, Regulatory, Manufacturing, and Legal.
- Provide medical review to global promotional and non-promotional materials.
- Represent the company with external scientific leaders, patient advocacy groups, and/or regulatory authorities.
- Support strategic partnerships with centers of excellence and KOLs.
Position Accountabilities:
- Lead development/implementation of short- and long-term medical strategies (scientific communication, evidence generation, capability building, KOL engagement).
- Develop global medical plans and pre-/post-launch tactics; manage in-year medical budget and plans.
- Oversee functional plans (publications, medical communications, medical information, medical training).
- Collaborate with business partners to align brand strategy and execution; provide medical affairs/R&D inputs.
- Plan/manage global Advisory Boards; track/manage KOL engagement activities in the KOL platform.
- Support global regulatory meetings; advise on regulatory information (e.g., Package Insert, Patient Information).
- Support clinical research strategy, evidence generation (including Phase IV), and adverse event evaluation.
- Lead capability building with training/continuing education; partner on AI-driven projects.
Required Qualifications:
- Advanced scientific degree (MD preferred; PhD or PharmD).
- 7+ years pharmaceutical experience in Medical Affairs or Clinical Development/R&D or related functions at international level.
- Experience/training in benign hematology and bleeding disorders.
- Medical Affairs experience supporting brands/disease area internationally.
- Experience creating post-approval studies, medical strategies, and launch plans.
- Strong understanding of R&D critical processes and pharmaceutical regulations in key markets.
Additional Information:
- Travel: ~30%.
- Hybrid work.
Compensation/Benefits (as stated):
- U.S. base salary range: $192,400–$302,390.
- Eligible for incentives; medical/dental/vision, 401(k) match, disability, life insurance, tuition reimbursement, paid volunteer time off, holidays, well-being benefits, sick time, and vacation.
Application Instructions:
- Apply via the “Apply” button (application process begins; info processed per Privacy Notice and Terms of Use).