Consultant - Value, Access, and Pricing (VAP) London

Posted 13 Days Ago
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Lime Street, Malvern Hills, Worcestershire, England, GBR
In-Office
Mid level
Analytics • Biotech • Consulting • Pharmaceutical
The Role
Support EVAP teams by conducting payer/HTA and pricing analyses, literature and guideline reviews, value dossier development, primary research support, and creating client-ready slides and recommendations.
Summary Generated by Built In

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Company Profile
Trinity (www.trinitylifesciences.com) is a leading life sciences consulting firm that provides strategic and tactical insights to clients worldwide. Our clients are among the most successful firms in the industry and include a mix of pharmaceutical, biotechnology, medical device, and diagnostic companies. Blending consulting services with research capabilities, we specialize in corporate strategy, pipeline & portfolio optimization, brand planning, market analytics, promotional effectiveness, and licensing & acquisition. Based just outside Boston, MA, with offices in New York City, Princeton, San Francisco, Toronto, London and Gurgaon, Trinity has over 700 employees. Trinity is an EEO organization.
 

Position Summary
We are currently seeking a Consultant 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, and value dossier development.

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.

  • Conducting US payer analysis, understanding 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.

  • Analyze and synthetize findings into slides, supporting development of final recommendations to the client.

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

  • Provide engagement support and team management.

Position Requirements

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

  • 2.5+ years of research experience in consulting, research organizations or related fields.

  • Knowledge and understanding of pricing and access systems and HTAs in Europe, USA, and developing countries.

  • Working knowledge of essential consulting methodologies, tools, and techniques.

  • Good analytical skills and numeric capability.

  • Ability to understand, interpret and communicate scientific content.

  • Strong oral and written communication skills in English language.

  • Ability using PubMed / Medline, Google Scholar, research platforms to source reimbursement and HTA data.

  • Proficiency in MS Office Suite (Microsoft Word, PPT, and Outlook).

  • General 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.

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

Trinity Life Sciences is an equal opportunities employer and welcomes applications from all qualified individuals. At Trinity, inclusion and engagement are at the heart of how we work and grow together. We’ve evolved from a traditional “DEI” framework to Inclusion & Engagement (I&E)—a model that moves beyond representation to focus on connection, collaboration, and shared purpose. Every role at Trinity plays a part in fostering an environment where all employees feel valued, respected, and empowered to contribute fully. By embedding I&E principles into our culture, we ensure that belonging and engagement are not standalone initiatives—they are part of how we build teams, make decisions, and deliver excellence every day. Trinity will not tolerate any form of discrimination or harassment and encourages applicants of all ages and identities. For more information about Trinity’s commitment to Inclusion and Engagement please visit Inclusion & Engagement | Culture of Belonging at Trinity Life Sciences.

Skills Required

  • Bachelor's degree with high academic achievement
  • Major in health sciences, Economics, HEOR, or demonstrated interest in life sciences
  • 2.5+ years of research experience in consulting, research organizations or related fields
  • Knowledge and understanding of pricing and access systems and HTAs in Europe, USA, and developing countries
  • Working knowledge of essential consulting methodologies, tools, and techniques
  • Good analytical skills and numeric capability
  • Ability to understand, interpret and communicate scientific content
  • Strong oral and written communication skills in English
  • Ability using PubMed / Medline, Google Scholar, research platforms to source reimbursement and HTA data
  • Proficiency in MS Office Suite (Microsoft Word, PPT, and Outlook)
  • General 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
  • Ability to work under the pressure of deadlines and manage multiple priorities
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The Company
1,672 Employees
Year Founded: 1996

What We Do

Trinity Life Sciences is a modern partner to companies in the life sciences industry with nearly 30 years of expertise. The firm combines strategy, insights, and analytics to help life science executives with clinical and commercial decision-making. Serving over 300 pharmaceutical, biotech, and medical device clients, Trinity helps them develop the right drugs and devices for today’s market and optimize them once in market.

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