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. ## 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 ## 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, 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 ## Nice to Have - Plot generation ## Benefits Please mention the word **SUAVELY** and tag RMmEwMTo0Zjg6MWMxNjplZThlOjox when applying to show you read the job post completely (#RMmEwMTo0Zjg6MWMxNjplZThlOjox). 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.