Associate Director, Content Strategy & Development (medical Writing)
Gilead Sciences
Dublin, Ireland
Extensive medical writing experience
Regulatory document submission knowledge
Proficiency in word adobe excel
The role involves preparing high-quality clinical documentation to support global pediatric regulatory submissions at Gilead Sciences
Job Summary
The role involves preparing high-quality clinical documentation to support global pediatric regulatory submissions at Gilead Sciences.
Candidates will independently author complex documents including protocols, CSRs, and integrated CTD summaries according to strict regulatory requirements.
The position offers opportunities to lead document timelines, develop standards, and mentor less experienced writers within a collaborative team.
Matching Summary
The role involves preparing high-quality clinical documentation to support global pediatric regulatory submissions at Gilead Sciences.
Skills & Requirements
Must-have
extensive medical writing experience
regulatory document submission knowledge
proficiency in Word Adobe Excel
Nice-to-have
cross-functional team collaboration skills
mentoring and coaching capabilities
strategic thinking for regulatory submissions
Key Requirements
BA/BSc or MA/MSc degree required
Direct experience with pediatric regulatory documents
Experience directing documents for regulatory submissions