AbbVie is seeking a Manager, Strategic HTA Writer to provide clinical EUHTA document support to the JCA core team, ensuring successful preparation of high-quality submission-ready documents and effective implementation of the clinical writing process.
Requirements
- A minimum of 3+ years of bio-pharmaceutical industry experience in global pharma, biotech, life science, HTA agency organization delivering medicines/therapies to a broad market across various therapeutic areas.
- Extensive experience in writing HTA dossiers, eg AMNOG, HAS, NICE, CDA dossier preferred.
- Bachelor's Degree or higher in a scientific discipline.
- Outstanding written and oral communication skills, with a comprehensive knowledge of medical and scientific terminology across multiple therapeutic areas.
- Proficient in assimilating and analyzing complex data.
- Advanced understanding of HTA dossiers and HTA requirements, clinical research, study designs, biostatistics.
- Good understanding of regulatory requirements, and medical terminology cross functional teams and multiple contributors.
- Excellent English writing skills, effectively communicate and influence complex scientific and medical information to various stakeholders.
- Ability to collaborate with cross-functional teams.
- Strong organizational, time management, and problem-solving skills.
