- Sales meetings
- Learning systems
- Objection/concern handlers
- Product flash cards
- Annotated clinical reprints/sales aids
- Train-the-trainer meetings
- Global launch meetings (product, indication, and patient/physician support program)
- Internal pharmacoeconomic reports and presentations
- Conference abstracts and posters
- Managing internal approval processes – brand, medical, regulatory, and legal review
- Developing content within the confines of the regional regulatory environment – US and Europe
- Content development in a variety of formats – print, PowerPoint presentation, and multimedia
- Maintenance of product branding and style – branding guidelines, AMA style, client style guides
- Comprehensive and accurate referencing – reference to page and paragraph within provided reference sources, familiar with company-specific referencing platforms
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