Associate Consultant - Evidence Strategy/HEOR Focus

Position Summary

We are currently seeking an Associate Consultant to support our Evidence, Value, Access and Pricing (EVAP) teams with research activities spanning across several adjacent areas: targeted and systematic literature reviews, clinical guidelines, epidemiology data, and value dossier development.

Position Responsibilities

- Conduct general secondary research activities such as review of clinical guidelines, epidemiology sources, treatment algorithms, product's reimbursement status across key markets

- Perform literature data search from multiple databases, including PubMed and EMBASE

- Execute review of selected publications, including quality control with second reviewer, while being able to extract relevant data

- Perform statistical analysis for the meta-analysis based on the feasibility assessment

- Perform meta-analysis based on data quality and availability, including plot generation (nice to have)

- 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

- Analyze and synthetize primary and secondary research data to feed into the development of a value dossier and related guidance / tool-kit materials

- Support execution of primary research programs (e.g., focus groups, IDIs) to pressure test, inform value story development, and exploring opportunities to investigate value proposition from competition.

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 - medical writing background preferred

- 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

- 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