Director, Epidemiology & RWE Sciences

Reposted 2 Days Ago
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Cambridge, MA, USA
In-Office
177K-260K Annually
Senior level
Healthtech • Manufacturing
The Role
Lead global epidemiology and real‑world evidence (RWE) strategy for oncology assets across the product lifecycle. Design and oversee prospective and retrospective RWE studies, develop integrated evidence plans, ensure regulatory and payer alignment, mentor teams, partner cross-functionally, and promote methodological innovation and data-driven insights to support regulatory, clinical, and market access decisions.
Summary Generated by Built In

Title:

Director, Epidemiology & RWE Sciences

Company:

Ipsen Biopharmaceuticals Inc.


 

About Ipsen:

Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation.

 Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

For more information, visit us at https://www.ipsen.com/ and follow our latest news on LinkedIn and Instagram.

Job Description:

The Director, Epidemiology and RWE Sciences will support pre- and post-launch evidence generating activities across all Oncology products. The role is responsible for leading the global evidence strategy and real‑world evidence generation for Ipsen’s oncology assets across the product lifecycle. This role provides scientific and strategic leadership to ensure that robust, fit‑for‑purpose RWE is generated to support regulatory, payer, clinical, and medical decision‑making, with a strong focus on high‑unmet‑need oncology indications.

The Director will define and execute integrated evidence plans (IEPs), oversee RWE studies (e.g., registries, retrospective and prospective observational studies, database studies), and partner closely with Global Medical Affairs, Clinical Development, Regulatory Affairs, Market Access, HEOR, Biostatistics, and Safety.

The role will be responsible for methodological epidemiological & RWE leadership and will contribute the development of new SOPs and guidance documents that will promote and ensure timely and high-quality, “fit-for-purpose” evidence generation. The Director will also take a lead in serving as a subject matter expert and in building capacity for RWE research across the business. The role operates in a global, matrixed environment and ensures evidence generation adheres to scientific, regulatory, and compliance standards.

WHAT - Main Responsibilities & Technical Competencies

Evidence Strategy and Leadership:

  • Partner effectively across the enterprise to support the identified evidence needs across Oncology and play a central role in designing Integrated Evidence Generation Plans (IEGPs) that address evidence gaps and contribute to the global Integrated Data and Evidence vision at Ipsen, ensuring alignment with product strategy, disease area priorities, and Ipsen’s broader evidence generation objectives.
  • Provide strategic input to shape evidence that addresses regulatory, HTA, payer, clinician, and patient needs.
  • In partnership with the Asset Teams, drive the RWE strategy per asset as part of IEGPs
  • Conduct critical review of RWE/Epidemiology studies designed by external service providers and/or cross-functional partners to ensure scientific robustness and alignment with strategic goals.
  • Ensure the fulfilment of timely, high-quality epidemiology/RWE sections of Regulatory documents for agencies worldwide, including submissions, RMPs, breakthrough or orphan designations, advisory committee briefing books, etc.
  • Support External Innovation and Business Development teams in assessment of external licensing opportunities by providing timely disease population assessments.
  • Partner with Clinical Development teams to provide Epi support for study design and planning activities.
  • Engage externally with academic collaborators, patient registries, data partners, and methodological experts to advance Ipsen’s evidence capabilities and scientific reputation.
  • Develop and review study protocols and statistical analysis plans in collaboration with Biometry, Medical and other internal stakeholders.
  • Stay informed and involved on the latest regulatory and methodological advances that expand and enhance the utility of RWE.
  • Educate and raise the awareness around epidemiologic methods and RWE and its potential in supporting Ipsen’s internal teams to generate buy-in across the organization
  • Mentor and provide functional leadership to RWE and evidence generation team members as applicable.

Real-World Evidence Generation:

  • Design prospective and retrospective pharmaco-epidemiology studies (including RWE studies) in the pre-/post-launch setting, including related to Regulatory post-approval commitments.
  • Develop and adopt robust, fit-for-purpose data generation and analytic methodologies that advance research goals across different life cycle management stages.
  • Drive the adoption of modern RWE methodologies and analytic techniques to generate impactful evidence in settings where conventional approaches may be limited.
  • Apply and champion innovative study designs and modern analytics, such as pragmatic approaches, hybrid designs, external control arms, advanced causal inference methods, and longitudinal disease modeling, as appropriate.
  • Oversee vendor‑led and internally led RWE studies, including protocol development, study governance, timelines, quality, and budgets.
  • Ensure methodological rigor while balancing scientific innovation, feasibility, and regulatory acceptability in oncological or rare disease contexts.
  • Leverage contemporary data analytic methods (e.g., advanced statistical modeling, real‑world data enrichment, linkage of disparate data sources, and exploratory use of machine‑learning–enabled approaches where appropriate) to generate novel insights.
  • Partner with Biostatistics, Data Science, and external vendors to ensure appropriate application and interpretation of advanced analytics within RWE studies.

Administration:

  • Provide budget input for activities related to Epidemiology and RWE studies and initiatives ensuring projects are adequately resourced.
  • Ensure all RWE activities comply with internal SOPs, global regulations, data privacy requirements, and ethical standards.
  • Actively participate in review of study proposals.
  • Provide seamless and consistent support to global and local franchises.
  • Ensure linkage of study data and insights gathered from external experts, including HCPs and patient organisations, in close continuous partnership with Medical Asset Leads and Therapy Areas.

Collaborate with internal Ipsen stakeholders on all topics around RWE:

  • Fully involve Ipsen stakeholders (GMA TAs, HEOR, GMA Clin Ops, GMPC, R&D and affiliates) in the design and implementation of the RWE framework utilizing strong communication skills.
  • Ensure Ipsen can provide comprehensive patient focussed data & analytics in the disease areas we serve.
  • Drive Medical, cross-functional and global alignment to enable early strategic alignment of Medical Affairs.
  • Epidemiology and RWE studies across global and local teams, in partnership with the Medical Asset Leads, to ensure late phase data generation plans maximise data availability, ensure patient impact and effective execution of RWE programs.
  • Establish end-to-end best practices for data generation and sharing (policy, SOP, Legal, Privacy, etc.).

HOW - Knowledge & Experience

Knowledge & Experience (essential):

  • Minimum 8-10 years of biotech/pharmaceutical experience in an Epidemiology, clinical RWE or outcomes research role within the pharmaceutical, biotech, or healthcare research environment
  • Strong methodological and analytical skills
  • Knowledge of medical, regulatory, and payor systems in one or more regions of the world
  • Demonstrated experience in designing and conducting pharmaco-epidemiology studies in support of pre-/post-approval evidence generating activities
  • Demonstrated experience applying innovative methodologies and modern analytic approaches to RWE, ideally in oncology, or specialty diseases
  • 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 ability to provide strong direct global project management/leadership skills
  • Exceptional critical thinking to help identify gaps, analyse findings and make recommendations while articulating next steps
  • Possession of core strategy and analysis skills, as well as the ability to lead and influence others by acting as a strategic partner to medical leaders
  • Applies emerging knowledge and trends; builds strong relationships; contributes to expertise within and beyond assigned area
  • Links responsibilities with the mission of the organisation; focusses on activities that add most value
  • Demonstrated ability to collaborate in a matrix and remote organizations
  • Ability to work, lead and thrive in a cross-functional team environment
  • Ability to work independently and as an active member within cross-functional teams
  • Demonstrated experience in innovative and design thinking
  • Cross-cultural awareness
  • Excellent verbal communication, written, interpersonal, presentation and influencing skills
  • Ability to prioritize effectively

Education / Certifications (essential):

  • Advanced degree in Epidemiology, Public Health, Health Outcomes Research, Pharmacoepidemiology, Biostatistics, Medicine (MD), or a related scientific discipline required.
  • PhD or MD/MPH strongly preferred.

Language(s) (essential):

  • Fluent in English.

Ipsen Biopharmaceuticals, Inc. is an equal opportunity employer. We recruit, employ, train, compensate, and promote without regard to race, religion, creed, national origin, age, gender, sexual orientation, sexual identity, marital status, military or veteran status, disability, genetic information, or any other category protected by applicable federal, state or local law.

Ipsen Biopharmaceuticals, Inc. conducts background screening, reference checks, and drug testing as part of its pre-employment screening process. This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. This position may change or assume additional duties at any time.  The employee may be requested to perform different or additional duties as assigned.

All Employees are expected to adhere to all company policies and act as a role model for company values.

The annual base salary range for this position is $177,000-$259,600.

This job is eligible to participate in our short-term incentives program as well as our long-term incentives program.

At Ipsen we are proud to offer a comprehensive employee benefits package, including 401(k) with company contributions, group medical, dental and vision coverage, life and disability insurance, short- and long-term disability insurance, as well as flexible spending accounts. Ipsen also provides parental leave, paid time off, a discretionary winter shutdown, well-being allowance, commuter benefits, and much more.

The pay range displayed above is the range of base pay compensation within which Ipsen expects to pay for this role at the time of this posting. Individual compensation within this range depends on a variety of factors, including, but not limited to, prior education and experience, job-related knowledge and demonstrated skills

We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application. Ipsen is an equal opportunity employer that strictly prohibits unlawful discrimination. We recruit, employ, train, compensate, and promote without regard to an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.

Skills Required

  • Minimum 8-10 years of pharmaceutical/biotech experience in Epidemiology, clinical RWE or outcomes research
  • Advanced degree in Epidemiology, Public Health, Health Outcomes Research, Pharmacoepidemiology, Biostatistics, Medicine (MD), or related scientific discipline
  • PhD or MD/MPH
  • Demonstrated experience designing and conducting pharmaco-epidemiology studies supporting pre-/post-approval activities
  • Strong methodological and analytical skills in epidemiology and RWE
  • Experience applying innovative methodologies and modern analytic approaches to RWE (e.g., external control arms, causal inference, hybrid designs)
  • Expertise in data collection methods and familiarity with secondary data sources and registries
  • Excellent data analytic skills, including knowledge of standard statistical software and packages (SAS, R)
  • Experience leading external analytic and evidence generation activities, including vendor oversight
  • Demonstrated ability to provide strong global project management and leadership
  • Knowledge of medical, regulatory, and payer systems in one or more regions
  • Exceptional communication, presentation, and influencing skills; ability to work cross-functionally in a matrix organization
  • Fluent in English
  • Experience with modern data analytics, linkage of disparate data sources, and use of machine‑learning-enabled approaches where appropriate
  • Cross-cultural awareness and ability to mentor and build capacity for RWE research

Ipsen Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Ipsen and has not been reviewed or approved by Ipsen.

  • Healthcare Strength Health coverage is described as comprehensive, with broad medical, dental, and vision offerings. Company materials emphasize a wide-ranging package that supports overall wellbeing.
  • Retirement Support Retirement programs are highlighted with a competitive 401(k) match and access to an employee stock purchase plan. These elements are frequently cited as strengths in the package.
  • Parental & Family Support Family support includes paid parental leave and company-provided backup child and elder care. These programs complement core benefits and add practical day-to-day value.

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The Company
HQ: Boulogne-Billancourt
5,848 Employees

What We Do

Ipsen is a French leading global mid-size biopharmaceutical company headquartered in Paris, France focusing its efforts where unmet medical needs are greatest. Ipsen develops and commercializes innovative medicines in three key therapeutic areas - Oncology, Rare Disease and Neuroscience. We have over 5000 employees worldwide and our medicines are registered in more than 100 countries, with direct commercial presence in over 30 countries. Ipsen has 4 global R&D hubs and 3 pharmaceutical development centers around the world

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