October 29
• Write complex scientific, clinical, and regulatory documents • Mentor more junior scientific writers • Write investigational medicinal product dossiers and clinical study reports • Compile and publish complex documents • Write patient narratives and other pharmacovigilance documents • Write and edit publications for peer-reviewed scientific/medical journals • Write abstracts, posters, and presentations for scientific congresses • Translate scientific articles and clinical documents • Perform reviews of the literature • Participate in review of statistical analysis plans • Maintain internal databases • Perform Quality Control or peer reviews of documents • Participate in marketing support • Ensure that document and standards timelines are met • Participate in creation and maintenance of document templates and SOPs
• At least 10 years of experience as a scientific writer • Experience mentoring more junior scientific writers • Graduate or post-graduate degree in medicine, pharmacy, or a scientific field • Fluent in English with excellent written proficiency in the language • Computer literacy (Word, PowerPoint, Excel) • A keen eye for detail and good communication skills • Ability to work independently (and remotely) and yet be a great team player • Flexible approach to work • Well organized and attention to detail while maintaining a “getting the job done” mentality • Client-focused • Focused on delivering high-quality results on time • Sensitive to cross-cultural differences.
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