Position Summary
We are currently seeking a Research Associate to support Trinityâs 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, productâs 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
- Bachelorâs degree with high academic achievement; major in health sciences, Economics, HEOR, and/or demonstrated interest in life sciences is a plus
- 1-4 years of research experience in consulting, research organizations or related fields â 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
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