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Dompe US - Global Medical Affairs

Job in Weymouth, Norfolk County, Massachusetts, 02188, USA
Listing for: Northeastern University
Full Time position
Listed on 2026-10-09
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
  • Research/Development
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 60000 - 85000 USD Yearly USD 60000.00 85000.00 YEAR
Job Description & How to Apply Below
Position: Dompe US - Global Medical Affairs - Real-World Evidence
Dompé US
- Global Medical Affairs
- Real-World Evidence &Health Economics and Outcomes Research Postdoctoral Research Fellow

Northeastern University Pharmaceutical Industry Fellowships Programis a two-year experiential program designed to advance lifelong learning and the education and training of Pharm.

D. graduates. Akey element of the program's success is preparing Fellows to meet evolving workforce needs across various sectors of the pharmaceutical industry. Fellows have the opportunity to work closely with our innovative biopharmaceutical industry partners, while engaging with Northeastern University faculty in professional and career development, teaching, service, and scholarly activities. In partnership with Northeastern University, Dompé is offering atwo-year fellowship in Global Medical Affairs
- Real-World Evidence& Health Economics and Outcomes Research (RWE/HEOR), based remotely.

About Dompé

Dompé is an Italian bio-pharmaceutical company that focuses on innovation, where a long tradition in the field of personal wellness goes hand-in-hand with a commitment to research and development to meet unsatisfied therapeutic needs. Established in1940 in Milan, Dompé has a manufacturing hub in L'Aquila, and offices in Naples, Italy, and Tirana, Albania. The company has approximately 1,000 employees. The US headquarters of Dompé isbased in San Mateo, CA, in the San Francisco Bay Area.

The Pharmacy Postdoctoral Fellow will join the Real-World Evidence/ Health Economics and Outcomes Research (RWE/HEOR) team for atwo-year commitment, where they will be immersed in a variety of Global Medical Affairs activities. Year 1 is a dedicated immersion in RWE/HEOR, with experience in integrated evidence generation plan(IEGP) development, RWE generation, HEOR strategy and analytics,health technology assessment, value dossier development, and payer engagement. Year 2 consists of two 6-month rotations in Global Medical Affairs functions, selected from:
Medical Engagement Strategy, Medical Communications, Medical Information &Operations, Patient Advocacy, and Field Medical. Throughout Year 2,the fellow will continue to dedicate approximately 25% of theirtime to the RWE/HEOR team, with the remaining time devoted to theactive rotation. The fellow will also have the opportunity to learn about various industry functions such as Research & Development(Clinical Development, Clinical Operations, Biostatistics),Regulatory Affairs, Pharmacovigilance, or the Commercial Organization through longitudinal projects.

The fellow will alsohave the opportunity to attend Medical Congresses. Rotations may be extended at the discretion of the rotation supervisor. Other rotations can be arranged based on availability and interest of thefellow.

Responsibilities
  • Manage the generation of foundational epidemiologic data forcross-functional partners across all therapeutic areas and functions
  • Learn the tasks, processes, and industry standards involved in conducting RWE, HEOR, and epidemiologic research activities
  • Assist in managing integrated evidence plans across therapeutic areas
  • Contribute to the design and execution of RWE and HEOR studies,including concept documents, protocols, statistical analysis plans,and study reports
  • Contribute actively to the development and launch of RWE/HEORstrategies within the team
  • Support development of global value dossiers, health technology assessment (HTA) submissions, and payer-facing value communication materials
  • Support health economic modeling (e.g., cost-effectiveness andbudget-impact models) and systematic literature reviews
  • Collaborate with cross-functional teams (regulatory, marketing,sales, legal, and clinical development) to communicate up-to-datedata generation plans and needs as a subject matter expert
  • Support the…
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