Associate Analyst

Role overview

Associate Analyst at Trinity Life Sciences

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

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

Preferred qualifications and skills

• 1-4 years of research experience in consulting, research organizations or related fields – medical writing background preferred

Employment details

• Location: India - Gurgaon

Additional role details

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