The medical writer will produce high-quality regulatory and scientific documents for medical device and pharma clients while collaborating with project teams. Responsibilities include managing project timelines, ensuring data accuracy, and participating in quality control checks.
The Senior Director will lead the Pharmaceutical Writing Services group, providing scientific and operational leadership for complex clinical submission programs and medical device clinical evaluations. They are responsible for authoring high-level regulatory documents, mentoring staff, and serving as a primary technical authority for clients and project teams.
