Associate Director, Health Economics & Outcomes Research - Epidemiology

As an Associate Director, Epidemiology, you will be responsible for leading our HEOR-epidemiology projects and activities to inform, support, and strengthen global development and commercialization activities. This role will entail the design of, overseeing the execution of, and reporting on results of observational studies, using their subject matter expertise in epidemiologic study design and methods. The candidate should have up-to-date knowledge of epidemiologic methods and work effectively in a cross-functional environment.

• Generating real-world evidence (RWE) in support of research, clinical development, regulatory filings, and commercialization;
• Developing and/or reviewing protocols and statistical analysis plans for the generation of RWE. This will be to assess incidence/prevalence of disease, natural history of disease, and burden of illness as well as treatment patterns and effectiveness of standard of care;
• Interacting with internal partners (medical affairs, clinical development, regulatory affairs, pharmacoepidemiology, etc.) to assess RWE needs and advise on feasibility and limitations of using of RWE to address knowledge gaps;
• Authoring epidemiology sections of regulatory documents (e.g., orphan drug designation application, BLA, etc.) based on a review of the literature and database analyses;
• Collaborating with HEOR colleagues to disseminate RWE in compliance with company, industry, and regulatory requirements;
• Working cross-functionally to drive the incorporation of RWE into global development strategies;
• Maintaining an up-to-date awareness of guidance documents and communications that may impact planning for and implementation of RWE strategies/studies;
• Collaborating with internal and Alliance partners on RWE studies and deliverables; building and maintaining constructive and productive relationships across the Alliance.

• Are at ease with an abundance of detail and complexity, yet mindful of the big picture.
• Ability to work cross-functionally and present to internal partners, including senior management;
• Have the highly developed ability to balance multiple projects and initiatives, prioritize them and implement them independently
• You thrive in a fast-paced environment.

To be considered for this you are required to have a Ph.D. in epidemiology, public health, health services research or related field. Your experience will also include 4+ years academic, pharma/biotech, or consulting experience. Experience with designing and drafting observational study protocols and statistical analysis plans using real-world data (e.g. administrative claims data, EMRs, registries). Advanced knowledge of statistical methods commonly used in the analysis of large electronic healthcare databases (e.g. survival analysis, propensity scores); knowledge of AI/machine learning is a plus as is experience in the oncology therapeutic area.

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.