Icf Medical Writing Program Manager
Core
Lead patient-centric medical writing programs with a focus on Informed Consent Forms (ICFs) to ensure flawless delivery and quality of documents for clinical research outcomes.
Role type
Senior Medical Writing Program Manager
Builds
Regulatory and plain language medical writing deliverables for clinical trials
Domain
Pharmaceutical/CRO industry, clinical research
Deliverable
client delivery
Required skills
Advanced project management, regulatory document development guidelines, budgeting and forecasting, resource management, mentoring junior staff
Preferred skills
Medical writing experience (Regulatory and/or plain language), pharmaceutical/CRO industry experience
Technologies
None stated
Responsibilities
Develop and adapt project plans and timelines, engage and manage client relationships, monitor project progress and provide status updates, mentor junior staff and ensure compliance with quality processes
Seniority
Senior, hands-on IC with leadership responsibilities
