Director of Medical Writing (NJ)

This medical writing expert role will assume overall responsibility for directing the development and implementation of the medical communication strategy for all regulatory submission documents for all assigned drug projects and work with assigned Senior Medical Writers and Submission team experts in developing and implementing the submission authoring strategy for all clinical sections.

• An advanced Degree in Science
• 8+ years of experience in the pharmaceutical industry
• 6+ years of experience in regulatory medical writing involving all clinical document types in more than one therapeutic area.
• Must have experience in electronic document management and electronic regulatory submissions, tools and standards.
• Strong leadership experience and the ability to mentor
• Excellent verbal and written communication skills
• Some travel may be required.

Must be a US citizen or Green Card holder.

All your information will be kept confidential according to EEO guidelines.