ICF Program Manager
Core
Lead patient-centric medical writing programs focusing on Informed Consent Forms (ICFs) to ensure flawless delivery and quality of documents for clinical research outcomes.
Role type
Senior IC Medical Writing Program Manager
Builds
Regulatory and plain language medical writing deliverables (ICFs) for clinical trials
Domain
Pharmaceutical/CRO industry, Clinical Research
Required skills
Project management, Client relationship management, Regulatory document development, Budgeting and forecasting, Resource management, Team mentorship
Preferred skills
Medical writing (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
