Education and Experience Required:
• Master’s degree in life sciences and 3+ years of medical writing experience at a medical device, biotechnology or contract research organization; or BS degree with 5+ years of experience
• Understanding of world-wide clinical related regulations and guidance documents.
• Expertise in MS Word, Excel and PowerPoint.
• Demonstrated analytical skills and interpretation of clinical data.
• Excellent verbal and written communication skills.
• Strong attention to detail and exceptional follow-through.
• Ability to interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management in the organization.
• Ability to work and excel within a fast-paced, dynamic, and continuously changing work environment.
• Solid project management and organizational skills with the capacity to prioritize and multi-task.