Associate Analyst

We're committed to bringing passion and customer focus to the business.

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.

Position 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 synthetize 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

Position 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

Please mention the word SUAVELY and tag RODUuMjE1LjE5OC4xMTI= when applying to show you read the job post completely (#RODUuMjE1LjE5OC4xMTI=). 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.