Associate Analyst

About the Role

Trinity Life Sciences is seeking a Research Associate to aid the Evidence, Value, Access, and Pricing (EVAP) teams. This role involves conducting comprehensive secondary research across multiple related fields such as targeted and systematic literature reviews, clinical guideline analysis, epidemiology data gathering, and contributing to value dossier creation.

Key Responsibilities

• Carry out secondary research including reviewing clinical guidelines, epidemiology data, treatment protocols, and reimbursement status of products in main markets.
• Retrieve relevant literature from databases like PubMed and EMBASE to support evidence synthesis.
• Critically assess published studies with a second reviewer for quality control and extract pertinent information.
• Perform statistical assessments to evaluate the feasibility of meta-analyses and conduct meta-analytical procedures with graphical data presentation when possible.
• Use gathered research insights to support developing value dossiers and frameworks tailored regionally and locally.
• Review previously created value dossiers and formulate draft value frameworks accordingly.
• Consolidate and interpret primary and secondary research inputs to build actionable value propositions and guide material development.
• Assist with primary research initiatives such as focus groups and in-depth interviews to validate and enhance value storytelling, including exploring competitor value propositions.

Qualifications and Skills

• Bachelor's degree notably in health sciences, economics, HEOR, or related fields with a strong academic record.
• Between 1 to 4 years of experience in research or consulting, preferably with medical writing exposure.
• Excellent verbal and written communication proficiency in English.
• Familiarity with literature search platforms such as PubMed/Medline and Google Scholar.
• Competent use of MS Office tools; foundational Excel skills required.
• Basic understanding of systematic reviews, clinical trial design, and clinical research regulations.
• Exceptional attention to detail alongside strong organizational and time management capabilities.
• Effective collaborator capable of working within cross-functional teams.
• Ability to manage multiple deadlines and tasks in a high-pressure work environment.