Associate Consultant/Consultant - Evidence/Value/Access/Pricing - Pharma/Healthcare

EVAP Associate Consultant / Consultant (Value, Access, and Pricing Focus)

Position Responsibilities :

- 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

- 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

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+ 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