Sr. Medical Writer
Neurocrine seeks an in-house Sr. Medical Writer. The Medical Writer participates as a member of the Regulatory Affairs/Medical Writing group and is held accountable for accurate and timely completion of assigned documents.
ESSENTIAL DUTIES AND RESPONSIBILITIES (include, but are not limited to):
Effectively writes, rewrites, and/or edits clinical study protocols, clinical study reports, and investigational brochures with minimal supervision.
Reviews , interprets, and reports data accurately in clinical study reports.
Manages and completes assigned medical writing projects within timelines.
Reviews and provides feedback on documents prepared internally.
medical writing liaison to document review teams.
BS in scientific discipline with a minimum of 7 years relevant experience or MS with 5 years relevant experience.
Requires strong analytical skills and the ability to interpret complex scientific and medical data clearly.
Ability to analyze medical data and interpret its significance to clinical data collection and reporting.
Very strong written and oral communication skills.
Ability to work independently under limited supervision.