Associate Analyst

ABOUT THE ROLE We're seeking a highly motivated Research Associate to support our Evidence, Value, Access and Pricing (EVAP) teams at Trinity. As a Research Associate, you will play a critical role in conducting research activities across several adjacent areas, including targeted and systematic literature reviews, clinical guidelines, epidemiology data, and value dossier development. WHAT YOU'LL DO As a Research Associate, your primary responsibilities will include: Conducting secondary research activities such as reviewing clinical guidelines, epidemiology sources, treatment algorithms, and product reimbursement status across key markets. Performing literature data searches from multiple databases, including PubMed and EMBASE. Reviewing selected publications, extracting relevant data, and performing quality control with a second reviewer. Performing statistical analysis for meta-analysis based on feasibility assessment. Conducting meta-analysis based on data quality and availability, including plot generation (desired skill). Utilizing research and review findings to lay the foundation for value dossier development. Reviewing and analyzing previous value dossiers, developing draft value frameworks, and adapting these at the regional and local level. Analyzing and synthesizing primary and secondary research data to feed into the development of a value dossier and related guidance/tool-kit materials. Supporting the execution of primary research programs, such as focus groups and IDIs, to pressure test and inform value story development. WHAT YOU'LL NEED To be successful in this role, you will need: A Bachelor's degree with high academic achievement; a major in health sciences, Economics, HEOR, or a demonstrated interest in life sciences is a plus. 1-4 years of research experience in consulting, research organizations, or related fields, with a medical writing background preferred. Strong oral and written communication skills in the English language. Ability and knowledge in using PubMed/Medline, Google Scholar, and other literature research platforms. Proficiency in MS Office Suite (Microsoft Word, PPT, and Outlook) and foundational knowledge of MS Excel. A general understanding of systematic review methods, clinical research design, and applicable standards and regulations for clinical trials. High attention to detail, superior organizational and time management skills. Ability to work as a strong team player with cross-functional staff. Ability to work under pressure of deadlines and manage multiple priorities. WHY REMOTE As a remote employee, you will have the flexibility to work from home and maintain a healthy work-life balance. Our remote work environment allows you to collaborate with our team members across the globe and contribute to our mission from anywhere. BENEFITS We offer a competitive salary and a range of benefits to support your career development and well-being.