Associate Analyst

Trinity Partners, LLC; India; On-site; INR 450,000 - 750,000; Full time

Job summary

Trinity Partners, LLC is seeking a Research Associate to support the EVAP teams in conducting literature reviews, epidemiology data gathering, and value dossier development. The role involves extracting data, performing meta-analyses where feasible, and contributing to evidence-based value frameworks across markets.

The candidate should have 1–4 years of research experience, strong English communication, and proficiency with PubMed/Medline, Google Scholar and MS Office.

Qualifications

• Bachelor's degree in health sciences, economics, HEOR or related field.
• 1–4 years of research experience in consulting or research organizations.
• Strong oral and written English communication skills.
• Proficient in PubMed/Medline, Google Scholar and literature databases.
• MS Word, PPT, Outlook; foundational MS Excel knowledge.
• Understanding of systematic review methods and clinical research basics.

Responsibilities

• Conduct literature reviews of guidelines, epidemiology and reimbursement status across key markets.
• Perform literature searches in PubMed/EMBASE and other databases.
• Review selected publications with data extraction and quality control.
• Conduct meta-analyses and generate plots as feasible.
• Contribute to value dossier development and research findings synthesis.
• Review prior value dossiers and assist in draft value frameworks for regional use.
• Support primary research programs (focus groups, IDIs) to inform value story development.

Skills

English communication

Team collaboration

Time management

Attention to detail

Education

Bachelor's degree in health sciences / economics / HEOR

Tools

PubMed/Medline

Google Scholar

MS Office (Word, PPT, Outlook)

MS Excel

Job description

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, 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