Senior ICF Project Manager
Core
Lead patient-centric medical writing projects focused on Informed Consent Forms (ICFs) for pharmaceutical and biotech clients, managing timelines, budgets, and resources to ensure timely delivery and quality.
Role type
Senior Informed Consent Form (ICF) Project Manager
Builds
ICF documents and related clinical trial deliverables for internal and external clients
Domain
Pharmaceutical / Biotechnology / Clinical Trials
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Project management, budgeting, forecasting, resource management, risk evaluation, quality compliance monitoring, contract modification liaison, cross-functional collaboration, regulatory guideline knowledge
Preferred skills
Medical writing experience, ICF content management, pharmaceutical/CRO industry experience, regulatory and plain language writing
Technologies
Tracking and management tools
Responsibilities
Develop project timelines, standards, budgets, and forecasts; collaborate with cross-functional teams to meet deliverables; monitor project status and provide escalation updates; evaluate and resolve risks to quality, budget, or timeline; ensure compliance with quality processes and regulatory guidelines
Seniority
Senior, hands-on IC
