Senior Medical Writer

hace 4 meses


Girona, España Almirall A tiempo completo

Mission

The Senior Medical Writer serves as a key contributor to regulatory and clinical projects, leveraging a scientific background and writing expertise to produce high quality strategic and operational documents.

Tasks and Responsibilities

Working with the project and trial teams, the Senior Medical Writer takes leadership responsibility for the timely authoring, review, finalization, and approval of regulated documents for development and marketed products. Documents may include but are not limited to electronic Common Technical Document (eCTD) modules, health authority briefing packages, and clinical trial operational documents (eg, protocols, lay summaries, Investigator Brochures). Contributes to the creation and implementation of robust systems for document development and management. Serves as the medical writing content expert to regulatory and clinical development teams, including trial and project teams.

Education & Experience

Bachelor's degree (physical or biological sciences) with 5 years of relevant experience MS with 4 years of experience Doctoral-level degree (eg, PhD, MD, DVM, DO, PharmD) with 3 years of relevant career experience.

Skills

English fluency required, level C2 or native speaker preferred Demonstrated ability to understand and apply scientific concepts Good understanding of statistical principles

Values

Care Courage Innovation Simplicity
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