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We are currently seeking a Senior Manager to support Trinity’s Evidence, Value, Access, and Pricing (EVAP) teams with research activities spanning across several adjacent areas: Payer / HTA and pricing analysis, clinical guidelines, targeted and systematic literature reviews, value dossier development, and project management.

Position Responsibilities

  • Perform Payer / HTA analysis, extracting key insights from prior HTA reports across markets and archetypes (focus on Europe, Canada, other HTA-oriented countries) to inform initial hypothesis and recommendations.

  • Conduct US payer analysis, understand US payer nuances (e.g., payer prior authorization and tiering), and related access considerations; ASP & WAC price tracking; extraction of key utilization management criteria from payer policies.

  • Identify must-have versus nice to have evidence in manufacturers’ payer / HTA submissions.

  • Execute pricing analyses across geographies and to account for diverse pricing build-ups.

  • Review clinical guidelines and literature – understanding to inform treatment practices with an eye to evolution of clinical algorithms and payer comparator requirements.

  • Utilize research and review findings to lay the foundation for value dossier development.

  • Review and analyze previous value dossiers, while developing draft value frameworks, and adapting these at the regional and local level.

  • Based on research material, assist in the development of primary research documents with relevant payer authorities, and help the team executing program accordingly.

  • Synthetize findings into slides, including support in developing final recommendations to the client.

  • Develop logical, clear, and visually impactful communication materials.

  • Provide engagement support and team management.

  • Bachelor’s degree with high academic achievement; major in health sciences, Economics, HEOR, and / or demonstrated interest in life sciences is a plus.

  • 8+ years of research experience in consulting, research organizations or related fields – medical writing background preferred.

  • Demonstrated experience in team and project management.

  • Strong oral and written communication skills in English language.

  • Ability and knowledge in use PubMed/ Medline, Google Scholar, other literature research platforms

  • Proficiency in MS Office Suite (Microsoft Word, PPT, and Outlook); Foundational knowledge of MS Excel is required.

  • Understanding of systematic review methods, clinical research design, and applicable standards and regulations for clinical trials.

  • High attention to detail with superior organizational and time management skills.

  • Strong team player, ability to work with cross-functional staff.

  • Able to teach & train more junior team members.

  • Ability to work under the pressure of deadlines and manage multiple priorities.

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