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Ferring Pharmaceuticals

Develops peptide hormone-based medicines and therapies

Data Generation & Publication Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeTokyo, JapanNo salary listedIn-person

About the Job

Requirements

  • MD, Ph.D., or PharmD in a medical specialty, or an equivalent combination of experience and education.
  • At least 2 years of medical experience in the therapeutic area from a hospital, clinic, university, research industry, or pharmaceutical industry.
  • Business fluency in English and Japanese.
  • Ability to understand complex scientific information and communicate it effectively.
  • Strong scientific acumen and demonstrated scientific mastery in prior therapeutic areas of focus.
  • Ability to understand and interpret data, form independent opinions, and discuss findings with key external experts.
  • Ability to write medical papers to a limited extent.
  • Understanding of affiliate organization strategic needs.
  • Strong interpersonal skills for ongoing interaction with key external experts, physicians, patient organizations, and internal stakeholders.
  • Ability to present at congresses, advisory board meetings, and one-on-one meetings.
  • Ability to build long-term relationships with key external experts and physicians.
  • Strong planning and organizational skills, with ability to work effectively with limited oversight.

Responsibilities

  • Lead development and execution of evidence-generation plans addressing 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 studies, real-world evidence studies, registries, database studies, and other post-marketing research initiatives.
  • Align evidence-generation activities with medical strategies and business priorities through collaboration with Therapeutic Area Medical Affairs, Market Access, and regional and global stakeholders.
  • Drive innovation in evidence-generation methodologies to maximize the value and impact of scientific evidence.
  • Lead study concept development, protocol design, feasibility assessments, and operational planning.
  • Oversee company-sponsored study execution, ensuring timely study milestones, high-quality data generation, and regulatory compliance.
  • Support scientific review and governance of Investigator-Initiated Studies and collaborative research projects.
  • Monitor study progress, identify risks, and implement mitigation strategies to ensure successful study completion.
  • Lead 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 publication development.
  • Facilitate timely dissemination of scientific evidence to healthcare professionals, academic communities, and other stakeholders.
  • 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, Medical Science Liaisons, Market Access, and regional and global functions to identify evidence needs and translate findings into strategic recommendations.
  • Promote scientific excellence and methodological rigor across evidence-generation activities.
  • Represent evidence generation within cross-functional teams and strategic initiatives.
  • Partner with Office Medical Affairs, Medical Science Liaisons, Market Access, Regulatory Affairs, Pharmacovigilance, Clinical Development, and regional and global Medical Affairs teams.
  • Provide scientific and methodological expertise to support evidence-based organizational decisions.
  • Collaborate with external investigators, study sites, academic institutions, contract research organizations, and other research partners.
  • Oversee selection, management, and performance of contract research organizations, 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.
  • Develop and manage evidence-generation and publication budgets in alignment with strategic priorities and organizational goals.
  • Allocate financial and operational resources efficiently 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.
  • Foster expertise in epidemiology, outcomes research, medical writing, publication planning, and evidence-generation methodologies.
  • Promote scientific excellence, collaboration, accountability, and continuous improvement.
  • Build organizational capabilities to support future evidence-generation needs and strategic priorities.
  • Ensure research and publication activities comply with applicable regulations, ethical standards, company policies, Good Clinical Practice requirements, and industry guidelines.
  • Maintain oversight of publication governance and scientific integrity processes.
  • Ensure inspection and audit readiness for evidence-generation activities.
  • Promote transparency and responsible scientific communication in accordance with international publication standards.

Desired Qualifications

  • Experience formulating and executing clinical studies.

About the Company

Ferring Pharmaceuticals

Develops peptide hormone-based medicines and therapies

Ferring Pharmaceuticals develops medicines that use the body's own peptide hormones, focusing on specialties such as reproductive health, gastroenterology, and urology. Its products range from hormone-based therapies to newer gene-based treatments, such as Adstiladrin for bladder cancer. The company achieves its solutions through research-driven development and manufacturing, including synthetic production of peptide hormones (historically oxytocin and vasopressin) and ongoing expansion of production and clinical programs. Ferring differentiates itself by remaining privately held to pursue a long-term research vision, growing through organic expansion and strategic acquisitions while maintaining a global footprint (over 100 countries, 7,000+ employees). Its goal is to advance therapies that leverage the body's biology to treat diseases more effectively, supported by a sustained investment in R&D and manufacturing, with a future focus on bioengineered and gene-based approaches.

Company size
5,001-10,000
Company stage
Debt Financing
Total funding
$302.5M
Headquarters
Saint-Prex, Switzerland
Founded
1950

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