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Global Medical Affairs Lead, Plasma-Derived Therapies Innovations

5+ years
Not Disclosed
10 Nov. 27, 2024
Job Description
Job Type: Full Time Education: MSc./M. Pharm/PhD/MD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Description: Global Medical Affairs Lead, Plasma-Derived Therapies Innovations
Location: Flexible (Global Role)

About Takeda:
At Takeda, we are a forward-looking, world-class R&D organization dedicated to delivering transformative therapies to patients. Our focus on innovation spans across four therapeutic areas, and we are committed to bringing life-changing therapies to patients globally. Takeda is a certified Global Top Employer, fostering an inclusive, collaborative workplace that encourages innovation and empowers employees to grow through meaningful work.

Role Overview:
The Global Medical Affairs Lead for Plasma-Derived Therapies (PDT) Innovations will lead the development and execution of the global medical strategy for device and digital innovations within the PDT therapeutic area. This role will oversee the multi-year strategy for devices, digital assets, and related innovations that extend beyond Primary Immunodeficiencies (PID) into other therapeutic areas like SID and CIDP. You will serve as a global expert for the PDT portfolio, guiding scientific communications, educational materials, and external stakeholder engagement.

How You Will Contribute:

  • Global Medical Strategy Leadership:

    • Lead the development and execution of a multi-year global medical strategy for device and digital innovations, with a focus on expanding current PID areas into SID and CIDP.
    • Define and implement a strategy for publications, congress activities, HCP interactions, and scientific communication platforms to support the PDT portfolio.
    • Create educational materials that differentiate SCIG products and promote individualized treatment approaches using digital technologies and device innovation.
  • Stakeholder Engagement & Education:

    • Lead global advisory boards, steering committees, and 1:1 KOL engagements during congresses and other face-to-face or virtual meetings.
    • Build and manage relationships with external stakeholders, including KOLs, patient advocacy groups, scientific societies, and Centers of Excellence (CoEs).
    • Collect insights from internal stakeholders (e.g., LOCs, GCMU) to inform global medical strategy.
  • Cross-functional Collaboration & Internal Capacity Building:

    • Collaborate with cross-functional teams (R&D, clinical, regulatory, GEO, safety, compliance) to ensure alignment on strategy and execution.
    • Develop and execute scientific training strategies for internal teams, leveraging platforms like Takeda Plasma University.
  • External Representation & Compliance:

    • Serve as a senior company representative, interacting with external scientific leaders and regulatory authorities as appropriate.
    • Collaborate with Legal, Compliance, and Regulatory teams to ensure ethical interactions between PDT Global Medical Affairs personnel and external stakeholders.
    • Lead and plan company-sponsored and collaborative studies, including Phase IIIb/IV, disease registries, and epidemiological studies, in collaboration with clinical teams.
  • Budget Management & Reporting:

    • Provide input into the PDT R&D medical budget and manage the product/disease area medical budget.
    • Monitor progress against the medical plan and adjust strategies as necessary based on evolving disease area requirements.

Minimum Requirements/Qualifications:

  • Education & Experience:

    • A medical degree (MD), PharmD, PhD, or country-specific equivalent is required.
    • At least 5 years of experience in pharmaceutical medicine/medical affairs, with a focus on rare diseases (e.g., neurology, immunology).
    • Minimum 3 years of experience in global/international medical affairs.
    • Experience leading teams and working cross-functionally with R&D, clinical, regulatory, and commercial teams.
    • Clinical experience in immunology, neurology, hematology, or devices preferred.
    • Field-based experience (e.g., Medical Science Liaison or Medical Director) is a plus.
    • Experience in clinical development preferred.
  • Skills & Expertise:

    • Strong understanding of rare diseases and immunology.
    • Proven leadership skills in driving global medical strategies and stakeholder engagement.
    • Ability to interpret and communicate complex scientific data to various audiences.
    • Strong interpersonal and communication skills, with the ability to build relationships across functions and external partners.
  • Travel Requirements:

    • Availability to travel up to 30% of the time.
    • Some activities may require early or late meetings and attendance at scientific meetings during holidays and weekends.

Why Takeda:
At Takeda, we are committed to transforming patient care through the development of novel therapies and patient support programs. We value innovation, excellence, and diversity in our workforce, providing employees with stimulating careers and opportunities for growth. Join us to be part of an organization that is dedicated to improving health and creating a brighter future for patients around the world.

EEO Statement:
Takeda is an equal opportunity employer, ensuring a diverse and inclusive work environment. All employees and applicants are treated fairly, without regard to race, color, religion, sex, sexual orientation, gender identity, age, disability, or any other protected characteristic.

Apply now to lead the future of Plasma-Derived Therapies and digital innovation at Takeda.

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