Senior Consultant- Medical Writer

Additional details

• We're committed to bringing passion and customer focus to the business.
• Developing high-quality, scientifically accurate deliverables (manuscripts, abstracts, posters, slide decks, value dossiers, payer decks, objection handlers, HTA-related materials) aligned with client objectives and Trinity standards.
• Leading end-to-end content development across multiple projects/brands, from scoping and outline creation through drafting, review incorporation, and finalization within agreed timelines and budgets.
• Conducting targeted literature searches (PubMed, EMBASE, Google Scholar, HTA databases, guidelines, epidemiology sources) and synthesizing clinical, HEOR, and real‑world evidence into clear narratives and value stories.​ Translating complex clinical and economic data into compelling value‑focused messages and visualizations for diverse stakeholders (HCPs, payers, internal commercial teams, and other decision makers).
• Partnering closely with cross‑functional teams (consultants, health economists, statisticians, real‑world evidence teams) to shape overall evidence strategy and ensure alignment of content with project objectives.
• Providing scientific and strategic input into client discussions, workshops, advisory boards, and tactical planning, including live participation in client/KOL meetings as needed.
• Reviewing and quality‑controlling scientific content drafted by junior writers or other team members to ensure accuracy, consistency, compliance, and adherence to style/branding guidelines.
• Mentoring and coaching junior medical writers (and/or trainees) on scientific content, structure, referencing, and best practices in medical writing and evidence communication.
• Ensuring all deliverables comply with relevant industry codes, publication/HTA requirements, and client SOPs, and that referencing and data traceability are robust and audit‑ready.
• Proactively managing deliverables across multiple concurrent projects, communicating risks or timeline issues early, and contributing to efficient internal review and approval cycles.