Medical Writer

Job Summary

Supporting the clinical development organization in a remote work model, the full-time Medical Writer will develop clinical study documents, manage document completion, and lead document activities across therapeutic areas.

Key responsibilities

• Develop clinical documents including study reports, protocols, and informed consent forms
• Manage and facilitate document completion with oversight from Medical Writing leads
• Lead document activities for assigned compounds and drive document development meetings

Required qualifications

• Bachelor's degree; advanced degree preferred
• 1 year of relevant experience in medical writing or clinical research
• Awareness of the clinical research process and applicable regulations
• Experience with internal standards, procedures, and peer-review practices
• Working knowledge of Microsoft Word, Adobe Acrobat, and PowerPoint