Head of Evidence Generation - International Region

Ipsen

Paris

Sur place

EUR 90 000 - 130 000

Plein temps

14 jours+
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Résumé du poste

A dynamic biopharmaceutical company in Paris is seeking a Head of Evidence Generation to lead the development of the International evidence generation strategy. This role is pivotal in shaping high-quality clinical and real-world evidence that informs decision-making. The ideal candidate will have an advanced degree in life sciences, extensive experience in medical affairs, and a proven track record in leading evidence generation strategies. Strong leadership and data analytic skills are essential. This position offers opportunities for collaboration and innovation in a patient-focused environment.

Qualifications

  • Extensive experience in medical affairs, clinical research, RWE or HEOR within the pharmaceutical industry.
  • Proven track record in leading regional or global evidence generation strategies.
  • Experience with RWE, observational studies, and regulatory-grade data generation.

Responsabilités

  • Develop strategies for evidence generation at International to support clinical evidence gaps.
  • Oversee planning, execution, and reporting of evidence generation projects.
  • Ensure that the Global IEGP is well implemented at the local level.

Connaissances

Leadership
Strategic planning
Data analysis
Collaboration
Communication

Formation

Advanced degree in life sciences or related field (MD, PharmD, PhD preferred)

Outils

SAS
R

Description du poste

Are you ready to lead and innovate in a dynamic, patient-focused biopharmaceutical company?

Ipsen is a growing global specialty-driven biopharmaceutical company focused on innovation and specialty care. We aim to make a sustainable difference by significantly improving patients’ health and quality of life, providing effective therapeutic solutions for unmet medical needs through differentiated and innovative medicines in Oncology, Neurosciences, and Rare Diseases.

Why Ipsen?
  • Patient-Focused: The patient is at the heart of everything we do, and improving their outcomes is the deliverable of every strategy.
  • Employee Care: We care for our employees, who are the ambassadors making a real difference.
  • Bold Leadership: We attract and develop bold, agile, entrepreneurial individuals who take full ownership of their decisions.
  • Growth Opportunities: We offer a wealth of fulfilling challenges and growth opportunities in a fast-moving, game-changing organization.
About The Role

The Head of Evidence Generation – International will lead the development and direction of the Ipsen International (EX US & Canada) evidence generation strategy (Phase IV, ISS, RWE) to support Ipsen's medical objectives across all therapeutic areas (Oncology, Rare diseases and Neurotoxins).

This role is pivotal in shaping and delivering high-quality clinical and real-world evidence (RWE) that informs decision-making, supports access, and enhances patient outcomes.

The role requires strong leadership, scientific rigor, and cross-functional collaboration to ensure alignment with global strategies and local market needs.

Key Responsibilities
Strategic Leadership
  • Responsible for developing strategies for evidence generation (Phase IV, ISS, RWE) at International that support healthcare clinical evidence gaps and the LCM of our products
  • Assess the local needs and build proposal for scaling RWE capabilities (HC, resources, operating model) at International countries
  • Define and implement the International Evidence Generation Plan (IEGP) in alignment with global medical strategies and local evidence needs.
  • Provide budget input for activities related to Epidemiology and RWE studies and initiatives ensuring projects are adequately resourced
Evidence Generation Execution
  • Ensure that the Global IEGP is well implemented at local level and the country data gaps are well integrated in the IEGP (Global & Local) in alignment with lifecycle management (LCM) priorities
  • Oversee the planning, execution, and reporting of evidence generation projects (clinical studies, RWE, health outcomes research) across the region.
  • Ensure scientific, ethical, and regulatory standards are met in all research activities
  • Support country teams in project design and EGRB submission readiness
  • Cross-Functional Collaboration
  • Partner with Country medical directors, asset medical leads, market access, clinical operations, and HEOR to align evidence generation with business objectives
Capability Building
  • Lead the development of RWE capabilities at the Local/regional level, including operating models, resources, and trainings
External Engagement
  • Identify key research opportunities, including clinical studies, real-world evidence projects, and health outcomes research and foster partnerships and collaborations with institutions at International
  • Proactively identify, evaluate, and secure access to high-quality external data sources
Qualifications
  • Advanced degree in life sciences, medicine, epidemiology, or related field (MD, PharmD, PhD preferred)
  • Extensive experience in medical affairs, clinical research, RWE or HEOR within the pharmaceutical industry
  • Proven track record in leading regional or global evidence generation strategies
  • Experience with RWE, observational studies, and regulatory-grade data generation
  • Demonstrated strong leadership and experience in designing and conducting Phase IV, pharmaco-epidemiology studies in support of pre-/post-approval evidence generating activities;
  • Expert in data collection methods and strong familiarity with secondary data sources;
  • Experience leading external analytic and evidence generating activities;
  • Excellent data analytic skills, including knowledge of standard statistical software & packages (SAS, R, etc.);
  • Demonstrated experience in innovative and design thinking
  • Demonstrated ability to collaborate in a matrix and remote organizations
  • Exceptional critical thinking to help identify gaps, analyze findings and make recommendations while articulating next steps;
  • Deep understanding of international regulatory and payer evidence requirements
  • Excellent communication and stakeholder engagement skills
  • English fluency
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