Job Details

ID #53225562
Estado Massachusetts
Ciudad Cambridge
Tipo de trabajo Full-time
Salario USD TBD TBD
Fuente Bicycle Therapeutics
Showed 2025-01-07
Fecha 2025-01-07
Fecha tope 2025-03-08
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Senior Director, Global RWE/HEOR Lead

Massachusetts, Cambridge, 02138 Cambridge USA
Aplica ya

The Senior Director, Global Real-World Evidence (RWE) and Health Economics and Outcomes Research (HEOR) Lead will be responsible for building, leading the function within medical affairs, and cultivating partnerships with cross-functional leaders in clinical development, program management, legal, regulatory, and commercial. As an essential part of this growing organization, this role will oversee the strategy and execution of activities that are integral to developing and disseminating the clinical, humanistic, and economic value proposition of our therapies. This role will work to ensure that patients can have maximized access to our therapies by generating and communicating evidence to support registration, inform healthcare decision-making, and appropriately educate payers on the value of our medicines. Developing effective collaboration and communication processes with internal and external stakeholders will be a key component of this role. This position will report into the VP, Head of Global Medical Affairs.Create and lead the RWE/HEOR function within medical affairsDevelop comprehensive RWE/HEOR strategic plans and budgets for assets in developmentDevelop clinical, humanistic, and economic value propositionsEvaluate gaps in product value propositions and identify strategies and activities to fill those gapsLead payer-focused research in the U.S. and ex-U.S. to obtain feedback on product profiles, value propositions, evidence gaps, and evidence generation plansDirect the design, conduct, and analysis of studies or other fit for purpose evidence generating activities including economic models (e.g., budget impact, cost-effectiveness) and other projects (e.g., chart reviews, systematic literature reviews, patient reported outcomes studies, payer dataset analyses) needed to secure reimbursement or differentiate our productsCollaborate with regulatory affairs to identify, evaluate, and execute real-world evidence-generating activities that could support regulatory filingsLead the external dissemination of RWE/HEOR-relevant information including publications, presentations, and professional society and payer communicationsAppropriately engage with various U.S. and ex-U.S. payers (including HTA submissions) to meet requirements required to secure reimbursementBe an integral part of various internal teams to lead cross-functional activities that enable evidence-based healthcare decision-makingOversee the development of a Global Value Dossier/AMCP Dossier in partnership with cross-functional colleaguesIdentify, engage, and manage external partners (vendors) to maximize strategic planning and execution of the workflows described abovePerform all activities in strict compliance with international governmental regulations and consistent with industry best practices and consensus recommendationsOccasional business travel required (20%)

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