Consultant, Evidence Strategy

Trinity Life Sciences

Consultant supporting Trinity's Evidence Strategy with research activities in life sciences. Conducting literature reviews and data analysis for value dossier development.

Posted 5/15/2026full-timeNew York City • Massachusetts, New York • 🇺🇸 United StatesMid-LevelSenior💰 $110,000 per yearWebsite

About the role

Key responsibilities & impact

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.

Requirements

What you’ll need

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 – 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.

Benefits

Comp & perks

Annual discretionary performance bonus

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

statistical analysismeta-analysisdata synthesisliterature reviewquality controldata extractionvalue dossier developmentclinical research designsystematic review methods

Soft Skills

strong oral communicationstrong written communicationanalytical thinkingattention to detail