Jean is a biopharmaceutical communications professional with nearly 20 years of experience in corporate and investor relations and clinical development (medical writing). She is an expert medical, science, and business writer for print, web, and video; an experienced strategic communications advisor to senior management and global cross-functional teams for external and internal initiatives; and a skilled project leader for collaboration programs with U.S. and global colleagues. She has most recently worked on programs in oncology and endocrine rare diseases, with prior experience in cardiovascular diseases (devices), neurology, and gastroenterology.
CAPABILITIES
Corporate and Investor Relations
- Strategic communications plans. Corporate messaging and positioning. Website content. IR/PR agency selection and management. Medical conference and investor meeting/roadshow support.
- Media: Press releases. Q&A development. Fact sheets and backgrounders.
- Investors: Presentations. Earnings scripts and call preparation. SEC documents and annual reports. Corporate disclosure compliance.
- Crisis communications. Prior experiences include a corporate spin-off, shareholder activism and hostile tender offer process, strategic processes, corporate restructuring, asset sales, new partnerships and collaborations, and executive leadership changes.
Internal and Executive Communications
- Intranet and blog content. Editorial calendar planning.
- Video scripting and editing. Patient, KOL, and employee interviews. Videographer, photographer, and web design agency selection and management.
- Executive statements and town hall presentations.
Patient Advocacy and Clinical Trial Recruitment
- Disease awareness campaigns in collaboration with patient advocacy groups. Patient surveys, videos, social media outreach, and educational materials.
- Clinical trial branding and patient recruitment for Phase 2 and 3 trials. Landing pages, posters, postcards, and Q&As.
Medical and Science Writing
- Abstracts, posters, and presentations for scientific and medical conferences.
- Clinical trial protocols and amendments, investigator brochures, master informed consent forms, and clinical study reports.