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    FE

    Ferring Pharmaceuticals

    Pharmaceuticals

    Data Generation & Publication Manager

    Ferring Japan, JapanFull-time2+ yrs experiencePosted 3w ago
    All Ferring Pharmaceuticals jobs

    Job description

    Job Description:

    Key responsibilities:

    Evidence Generation Leadership

    • Lead the development and execution of evidence-generation plans that address critical scientific, clinical, health economic, and market access evidence gaps across the product lifecycle.
    • 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 initiatives.
    • Ensure evidence-generation activities align with medical strategies and business priorities through close collaboration with Therapeutic Area Medical Affairs, Market Access, and regional/global stakeholders.
    • 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 operational planning.
    • 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) and collaborative 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 publication development 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 healthcare landscapes.
    • Generate actionable insights from clinical studies, real-world evidence, and healthcare databases to support medical and business decision-making.
    • Collaborate with Office Medical Affairs, MSL, Market Access, and regional/global functions to identify 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-making across the organization.
    • Foster 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 external partners involved in evidence-generation activities.
    • Ensure high-quality project delivery, budget adherence, contractual compliance, and effective resource utilization.
    • 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 standards, 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:

    Required Education and Experience

    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:
    • Hospital / Clinic/University/Research Industry, or
    • Pharmaceutical Industry
    • Experience in formulating and executing clinical studies is preferred
    • Able to understand complex scientific information and communicate this effectively
    • 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

    Managers Competencies

    • Dealing with Ambiguity
    • Creativity
    • Innovation Management
    • Strategic Agility
    • Planning
    • Motivating Other
    • Building Effective Teams
    • Managing Vision and Purpose

    Location:

    Ferring Japan

    Job details are sourced from the employer's original posting.

    Open job posting
    FE

    About the company

    Ferring Pharmaceuticals

    A pharmaceutical company specializing in reproductive health, gastroenterology, and pediatric medicines.

    View all Ferring Pharmaceuticals jobs
    Industry
    Pharmaceuticals
    Open roles
    3

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