Medical Dossier Writer

My client, a leading global consultancy, is seeking an experienced Medical Dossier Writer to provide urgent support on a large-scale market access project.

You will support the development of high-quality medical dossier content, translating complex clinical evidence into clear, compelling and evidence-based narratives for a market access audience.

Responsibilities to include:

• Developing and writing medical dossier content covering clinical evidence, disease burden, unmet need and treatment pathways
• Reviewing and synthesising complex clinical and scientific evidence
• Supporting HTA submissions and related market access deliverables
• Conducting and/or contributing to systematic and targeted literature reviews
• Developing scientific narratives based on published evidence and other relevant data sources
• Supporting the development of manuscripts, abstracts, posters and other scientific communications where required
• Conducting KOL interviews and landscape research, incorporating insights into evidence-based narratives
• Working closely with internal teams and stakeholders to ensure accuracy, consistency and timely delivery
• Managing multiple workstreams and deadlines independently within a fast-paced project environment

Requirements:

• Experience in medical/scientific writing, ideally within market access, HEOR or pharmaceutical consultancy
• Experience across therapeutic areas such as Oncology, Rare Diseases and/or Ophthalmology
• Demonstrable experience writing medical dossiers and/or HTA submission materials
• Experience with NICE and/or other HTA submissions
• Strong understanding of clinical evidence, evidence synthesis and treatment pathways
• Experience translating complex clinical evidence into clear and compelling narratives
• Strong scientific literature review and evidence synthesis skills
• Experience working with KOLs and/or clinical experts
• Excellent written and verbal communication skills
• Proven ability to manage multiple projects, stakeholders and deadlines independently
• Experience with Joint Clinical Assessment (JCA) processes

Candidates should highlight any direct experience contributing to JCA-related work, European HTA submissions, clinical evidence packages or associated evidence-generation activities.

Engagement

This is an urgent requirement for support on a large-scale project, with the level and duration of involvement dependent on experience and availability.