Associate Analyst

We're committed to bringing passion and customer focus to the business.Position SummaryWe 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 ResponsibilitiesConduct general secondary research activities such as review of clinical guidelines, epidemiology sources, treatment algorithms, product’s reimbursement status across key marketsPerform literature data search from multiple databases, including PubMed and EMBASEExecute review of selected publications, including quality control with second reviewer, while being able to extract relevant dataPerform statistical analysis for the meta-analysis based on the feasibility assessmentPerform 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 developmentReview and analyze previous value dossiers, while developing draft value frameworks, and adapting these at the regional and local levelAnalyze and synthetize primary and secondary research data to feed into the development of a value dossier and related guidance / tool-kit materialsSupport 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 competitionPosition RequirementsBachelor’s degree with high academic achievement; major in health sciences, Economics, HEOR, and/or demonstrated interest in life sciences is a plus1-4 years of research experience in consulting, research organizations or related fields – medical writing background preferredStrong oral and written communication skills in English languageAbility and knowledge in use PubMed/ Medline, Google Scholar, other literature research platformsProficiency in MS Office Suite (Microsoft Word, PPT, and Outlook); Foundational knowledge of MS Excel is requiredGeneral 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 skillsStrong team player, ability to work with cross-functional staffAbility to work under the pressure of deadlines and manage multiple prioritiesPlease mention the word **SUAVELY** and tag RMmEwMTo0Zjg6MWMxODo4ODc5Ojox when applying to show you read the job post completely (#RMmEwMTo0Zjg6MWMxODo4ODc5Ojox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.