Associate Consultant
Company Profile
Trinity () is a leading life sciences consulting firm that provides strategic and tactical insights to clients worldwide. Our clients are among the most successful firms in the industry and include a mix of pharmaceutical, biotechnology, medical device, and diagnostic companies. Blending consulting services with research capabilities, we specialize in corporate strategy, pipeline & portfolio optimization, brand planning, market analytics, promotional effectiveness, and licensing & acquisition. We are currently seeking an Associate Consultant to support Trinity’s Evidence, Value, Access, and Pricing (EVAP) teams with research activities spanning across several adjacent areas: Payer / HTA (Health Technology Assessment) and pricing analysis, clinical guidelines, targeted and systematic literature reviews, and value dossier development.
Perform Payer / HTA analysis, extracting key insights from prior HTA reports across markets and archetypes (focus on Europe, Canada, other HTA-oriented countries) to inform initial hypothesis and recommendations.
· Conducting US payer analysis, understanding US payer nuances (e.g., Execute pricing analyses across geographies and to account for diverse pricing build-ups.
· Review and analyze previous value dossiers, while developing draft value frameworks, and adapting these at the regional and local level.
· Synthetize findings into slides, including support in developing final recommendations to the client
· Provide engagement support and team management.
Bachelor’s degree with high academic achievement; 1+ years of research experience in consulting, research organizations or related fields.
· Working knowledge of essential consulting methodologies, tools, and techniques.
· Ability to understand, interpret and communicate scientific content.
· Strong oral and written communication skills in English language.
· Ability using PubMed / Medline, Google Scholar, research platforms to source reimbursement and HTA data.
· Proficiency in MS Office Suite (Microsoft Word, PPT, and Outlook).
· General understanding of systematic review methods, clinical research design, and applicable standards and regulations for clinical trials.
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