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Director, Global Medical Lead, Zasocitinib – Psoriatic Arthritis; PsA)

Job in Kendall Square, Middlesex County, Massachusetts, USA
Listing for: USA - 3316 Takeda Development Center Americas, Inc.
Full Time position
Listed on 2026-10-04
Job specializations:
  • Healthcare
    Medical Science Liaison, Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 192400 - 302390 USD Yearly USD 192400.00 302390.00 YEAR
Job Description & How to Apply Below
OBJECTIVES:

Accountable for development, implementation, and ongoing optimization of the global medical strategy for zasocitinib in PsA, in alignment with the GMUH, Rheumatology, and enterprise strategy. Provide Director-level medical leadership and strategic counsel to the GPT, GMUH, Rheumatology, and senior cross-functional stakeholders on product profile, data interpretation, benefit-risk, evidence gaps, and external scientific dynamics. Lead the global PsA Medical Strategy Team and coordinate medical sub-teams and matrix partners to deliver integrated, high-quality, and timely execution.

Define the medical evidence and scientific communications plan; ensure insights from patients, HCPs, and external experts are systematically captured and translated into action. Enable consistent global-to-local medical strategy deployment in partnership with regional and affiliate medical teams, while recognizing local practice, access, regulatory, and stakeholder needs. Model Takeda values and a culture of scientific excellence, inclusive collaboration, compliance, accountability, and patient focus;

mentor and develop matrix colleagues as appropriate.

ACCOUNTABILITIES :

Serve as the global medical lead and single-point medical accountable leader for zasocitinib in psoriatic arthritis (PsA), reporting to the Global Medical Unit Head (GMUH), Rheumatology Partner with the GMUH, Rheumatology, to define and execute a multi-year global medical vision, integrated medical strategy, and evidence plan across the PsA lifecycle, aligned to the Global Project Team (GPT), product strategy, and evolving treatment landscape.

Translate deep understanding of PsA science, patient unmet need, and stakeholder insights into differentiated medical priorities, including launch preparedness, evidence generation, scientific communications, and lifecycle opportunities. Lead and influence a global, cross-functional medical matrix across Clinical Development, Regulatory, Pharmacovigilance, Commercial, Market Access, Health Economics and Outcomes Research (HEOR), Digital/Data & Technology (DD&T), regions, and affiliates to ensure medical leadership is embedded in key product decisions.

Chair or actively lead relevant Medical Strategy Team (MST) work streams and provide clear medical recommendations, risk assessments, and decision-making input to the GPT and senior governance forums. Establish measurable strategic priorities, milestones, and performance indicators; monitor execution, resolve barriers, and elevate material risks or trade-offs to the GMUH, Rheumatology, as appropriate.

Scientific Expertise, Evidence, and External Engagement

Act as the global scientific steward for zasocitinib in PsA, ensuring scientifically rigorous, balanced, compliant, and patient-centered medical content and external engagement. Shape and oversee the integrated evidence-generation strategy, including real-world evidence, investigator-sponsored research, data-generation partnerships, and publication priorities, in collaboration with Evidence Generation, Clinical, HEOR, and Publications colleagues. Build and sustain strategic relationships with international thought leaders, centers of excellence, professional societies, patient advocacy organizations, and other stakeholders to inform strategy and advance the scientific agenda.

Represent Takeda, as delegated, in high-impact scientific, medical, and policy forums; engage external experts credibly on complex PsA and zasocitinib data.

Medical Governance and Innovation

Provide senior medical review and approval input for global scientific and, where applicable, promotional and non-promotional materials in accordance with applicable policies, codes, and regulations. Ensure proactive identification and management of medical, evidence, safety, regulatory, and reputational risks across the PsA program. Champion responsible use of digital, data science, and AI-enabled approaches to strengthen insight generation, evidence planning, scientific exchange, and patient/HCP experience, consistent with governance and compliance requirements.

EDUCATION,

BEHAVIORAL COMPETENCIES AND

SKILLS:

Education & Experience Advanced scientific or clinical degree required: MD, DO, MBBS, PharmD, PhD, or equivalent advanced degree in a relevant life-science discipline. Medical degree and/or specialist experience in rheumatology, immunology, dermatology, or a related field strongly preferred. Typically 8–12+ years of progressively responsible experience in…

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