Associate Analyst

Trinity Life Sciences; Gurugram District; On-site; INR 600,000 - 1,200,000; Full time

Job summary

Trinity Life Sciences is seeking a Research Associate to support EVAP teams with literature reviews, epidemiology data and value dossier development. You will review clinical guidelines, perform database searches and extract data to feed into value frameworks.

The role requires 1–4 years of research experience, strong English communication, and proficiency with literature databases and MS Office. Collaboration with cross-functional teams and adherence to deadlines will be essential.

Qualifications

• Bachelor’s degree with high academic achievement in health sciences, economics, HEOR or life sciences.
• 1–4 years of research experience in consulting or research organizations; medical writing background a plus.
• Strong English written and oral communication skills.
• Experience using PubMed / Medline, Google Scholar and other literature databases.

Responsibilities

• Conduct secondary research including review of clinical guidelines, epidemiology sources, treatment algorithms and reimbursement status across key markets.
• Perform literature searches using PubMed and EMBASE.
• Review selected publications with quality control and data extraction.
• Perform meta-analysis based on feasibility and data quality; assist with plot generation (nice to have).
• Develop value dossiers foundations and regional/local frameworks and tools.
• Review and adapt prior value dossiers for regional relevance.
• Synthesize research data to feed into value dossiers and guidance materials.
• Support primary research programs (focus groups, IDIs) to test value propositions.

Skills

Literature research

English communication

MS Office proficiency

Data extraction

Education

Bachelor’s degree in health sciences / HEOR / economics

Tools

PubMed

Medline

Google Scholar

MS Excel

Job description

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