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