Generate content outlines that contain a clearly highlighted story arc and a complete reference list.
Develop client-ready drafts of content in various forms (slide decks, executive and comprehensive summaries, and other meeting materials).
Organize and annotate references in accordance with client’s directives.
Confer with the teams in the medical/legal/regulatory (MLR) review process, answer queries from the MLR review committee, and implement required changes.
Requirements
Advanced Science Degree (PharmD, MD, PhD) and 0-3 years of relevant experience
Proficiency in using Microsoft Word®, PowerPoint®, Excel®, Adobe Acrobat®, and reference-management software (e.g. EndNote®)