About the role
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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
Position Requirements
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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