We're committed to bringing passion and customer focus to the business.<br><br><strong>Position Summary<br><br></strong>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.<br><br><strong>Position Responsibilities<br><br></strong><ul><li>Conduct general secondary research activities such as review of clinical guidelines, epidemiology sources, treatment algorithms, product’s reimbursement status across key markets</li><li>Perform literature data search from multiple databases, including PubMed and EMBASE</li><li>Execute review of selected publications, including quality control with second reviewer, while being able to extract relevant data</li><li>Perform statistical analysis for the meta-analysis based on the feasibility assessment</li><li>Perform meta-analysis based on data quality and availability, including plot generation (nice to have)</li><li>Utilize research and review findings to lay the foundation for value dossier development</li><li>Review and analyze previous value dossiers, while developing draft value frameworks, and adapting these at the regional and local level</li><li>Analyze and synthetize primary and secondary research data to feed into the development of a value dossier and related guidance / tool-kit materials</li><li>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<br><br></li></ul><strong>Position Requirements<br><br></strong><ul><li>Bachelor’s degree with high academic achievement; major in health sciences, Economics, HEOR, and/or demonstrated interest in life sciences is a plus</li><li>1-4 years of research experience in consulting, research organizations or related fields – medical writing background preferred</li><li>Strong oral and written communication skills in English language</li><li>Ability and knowledge in use PubMed/ Medline, Google Scholar, other literature research platforms</li><li>Proficiency in MS Office Suite (Microsoft Word, PPT, and Outlook); Foundational knowledge of MS Excel is required</li><li>General understanding of systematic review methods, clinical research design, and applicable standards and regulations for clinical trials.</li><li>High attention to detail with superior organizational and time management skills</li><li>Strong team player, ability to work with cross-functional staff</li><li>Ability to work under the pressure of deadlines and manage multiple priorities</li></ul><br/><br/>Please mention the word **SUAVELY** and tag RMmEwMTo0Zjg6MWMxODo4YzUyOjox when applying to show you read the job post completely (#RMmEwMTo0Zjg6MWMxODo4YzUyOjox). This is a beta feature to avoid spam applicants. Com