Director, Scientific Writing
Core
Leading a high-performing scientific writing function to deliver rigorous research outputs for global and US Oncology Medical Affairs, including protocols, study reports, and manuscripts for interventional and real-world evidence studies.
Role type
Director, Scientific Writing (Management)
Builds
Scientific writing outputs (protocols, study reports, manuscripts, HTA dossiers) for Oncology clinical trials and observational studies.
Domain
Pharmaceutical / Oncology / Medical Communications
Required skills
Advanced degree in scientific/medical field, 7+ years scientific writing experience, drug development process knowledge, AI writing tools proficiency, budget and resource management, regulatory compliance (GPP/ICMJE)
Preferred skills
Oncology therapeutic knowledge, publication management systems, CMPP certification, AI-enabled workflow scaling experience
Technologies
Claude, Copilot, Gemini, ptimelylibraries
Responsibilities
Lead development of protocols and study reports for Phase II-IV interventional studies; Personally author and oversee scientific writing outputs for real-world evidence studies; Lead AI adoption roadmap for scientific writing; Lead budgets and contractor relationships; Collaborate with Evidence Delivery Team on deliverable planning; Represent team in CODE Leadership team
Seniority
Director, Management