Note: The job is a remote job and is open to candidates in USA. Trinity Life Sciences is a leader in life sciences commercialization, and they are seeking a Consultant to support their Evidence, Value, Access, and Pricing (EVAP) teams. The role involves conducting secondary research, performing literature data searches, executing statistical analysis, and developing value dossiers based on research findings.

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

Skills

• Bachelor's degree with high academic achievement; major in health sciences, Economics, HEOR, and/or demonstrated interest in life sciences is a plus
• 2.5+ years of research experience in consulting, research organizations or related fields
• 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
• Medical writing background preferred
• Meta-analysis based on data quality and availability, including plot generation (*nice to have*)

Benefits

• In addition to your base salary, you will also be eligible for an annual discretionary performance bonus.

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