Albion Rye Associates
Medical Dossier Writer
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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
- 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
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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
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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.
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