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Associate Analyst
Source: remoteok
Position Summary
We're committed to bringing passion and customer focus to the business. 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, and product 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 a second reviewer, while extracting relevant data.
- Perform statistical analysis for meta-analysis based on 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 explore opportunities to investigate value propositions from competition.
Position Requirements
- Education: Bachelor’s degree with high academic achievement; major in health sciences, Economics, HEOR, and/or demonstrated interest in life sciences is a plus.
- Experience: 1-4 years of research experience in consulting, research organizations, or related fields (medical writing background preferred).
- Communication: Strong oral and written communication skills in English.
- Research Skills: Ability and knowledge in the use of PubMed/Medline, Google Scholar, and other literature research platforms.
- Technical Skills: Proficiency in MS Office Suite (Microsoft Word, PPT, and Outlook); foundational knowledge of MS Excel is required.
- Knowledge: General understanding of systematic review methods, clinical research design, and applicable standards and regulations for clinical trials.
- Soft Skills:
- High attention to detail with superior organizational and time management skills.
- Strong team player with the ability to work with cross-functional staff.
- Ability to work under the pressure of deadlines and manage multiple priorities.