Lead the development and execution of evidence-generation plans that address critical
scientific, clinical, health economic, and market access evidence gaps across the product
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Design and oversee Phase IIIb/IV studies, health economics and outcomes research (HEOR), real
World evidence (RWE) studies, registries, database studies, and other post-marketing research
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Ensure evidence-generation activities align with medical strategies and business priorities
Through close collaboration with Therapeutic Area Medical Affairs, Market Access, and
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Drive innovation in evidence generation methodologies to maximize the value and impact of scientific evidence.
Study Strategy, Design & Execution
Provide leadership for study concept development, protocol design, feasibility assessments, and
Oversee the execution of company-sponsored studies and ensure timely delivery of study milestones, high-quality data generation, and regulatory compliance.
Support the scientific review and governance of Investigator-Initiated Studies (IISs) andcollaborative research projects.
Monitor study progress, identify risks proactively, and implement mitigation strategies to ensure successful study completion.
Publication & Scientific Dissemination
Lead the development and execution of integrated publication strategies aligned with evidence generation priorities and medical objectives.
Oversee publication planning, manuscript development, abstracts, congress presentations, and scientific communication activities.
Ensure scientific accuracy, transparency, quality, and compliance throughout the publicationdevelopment process.
Facilitate timely dissemination of scientific evidence to healthcare professionals, academic communities, and other stakeholders.
Scientific Excellence & Insights Generation
Monitor emerging scientific evidence, treatment trends, competitive developments, and evolving Generate actionable insights from clinical studies, real-world evidence, and healthcaredatabases to support medical and business decision-making.
Collaborate with Office Medical Affairs, MSL, Market Access, and regional/global functions toidentify evidence needs and translate findings into strategic recommendations.
Promote scientific excellence and methodological rigor across all evidence-generation activities.
Cross-functional Leadership & Collaboration
Act as the primary evidence-generation representative within cross-functional teams and strategic initiatives.
Partner closely with Office Medical Affairs, MSL, Market Access, Regulatory Affairs,Pharmacovigilance, Clinical Development, and regional/global Medical Affairs teams.
Provide scientific and methodological expertise to support evidence-based decision-makingundefinedFoster strong collaboration with external investigators, study sites, academic institutions,contract research organizations (CROs), and other research partners.
Vendor, CRO & External Research Management
Oversee the selection, management, and performance of CROs, research vendors, and externalpartners involved in evidence-generation activities.
Build and maintain productive relationships with external research collaborators and scientific organizations.
Budget Management
Develop and manage evidence-generation and publication budgets in alignment with strategic priorities and organizational goals.
Ensure efficient allocation of financial and operational resources across research and publication activities.
Monitor budget performance and contribute to annual planning, forecasting, and investment discussions.
Evaluate return on investment and strategic impact of evidence-generation initiatives to support future prioritization decisions.
People Leadership & Capability Development
Foster expertise in epidemiology, outcomes research, medical writing, publication planning, and evidence-generation methodologies.
Promote a culture of scientific excellence, collaboration, accountability, and continuous improvement.
Build organizational capabilities to support future evidence-generation needs and strategic priorities.
Governance & Compliance
Ensure all research and publication activities comply with applicable regulations, ethical tandards, company policies, GCP requirements, and industry guidelines.
Maintain oversight of publication governance and scientific integrity processes.
Ensure inspection and audit readiness for all evidence-generation activities.
Promote transparency and responsible scientific communication in accordance with international publication standards.
Required Experience & Competences
Minimum Education Requirements
MD, Ph.D., or PharmD in a medical specialty or equivalent combination of experiences and education
Minimum Experience Requirements
Min 2+ years of Medical experience in the TA from:
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Experienced in formulating and executing clinical studies is preferred
Able to understand complex scientific information and communicate this effectively
Team player with the ability to work under their initiative with a high work capacity by balancing priorities
Business fluency in English and Japanese
Other Posting information
Technical' Competencies
Scientific acumen: Strong technical skills with demonstrated scientific mastery in prior therapeutic areas of focus
Statistical & data interpretation: Need to understand and interpret data, form own opinion, discuss with KEEs
Medical paper writing: (Limited) need to write medical papers
Strategic acumen: Understanding the strategic needs of affiliate organization important for completion of tasks
Process-Related Core Competencies
Focus on scientific exchange: Excellent interpersonal skills; constant interactions with KEEs, physicians, patient organizations, and internal stakeholders.
Communicating effectively: Excellent communication skills; required to present at congresses, advisory board meetings, and one-on-one meetings
Relating skills: Strong need to build long-term relationships with KEEs and physicians
Process management: High level of planning and organizational skills; self-starters that are capable of working effectively with limited oversight