Associate Analyst

Position Summary We are currently seeking a Research Associate to support Trinity’s 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 synthesize 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 1-4 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, PowerPoint, 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 #J-18808-Ljbffr