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 or house style.
Confer with the teams in the medical/legal/regulatory (MLR) review process, answering all queries from the MLR review committee, and understand and implement the required changes.
Requirements
Advanced Science Degree (PharmD, MD, PhD)
2+ years of experience within a medical communications agency
In-depth knowledge of the criteria for development of various types of deliverables
Proficiency in using Microsoft Word®, PowerPoint®, Excel®, Adobe Acrobat®, and reference-management software (e.g. EndNote®)