Senior ICF Project Manager
Core
Lead patient-centric medical writing projects with a primary focus on Informed Consent Forms (ICFs) for internal and external clients in the pharmaceutical/biotech sector.
Role type
Senior ICF Medical Writing Project Manager
Builds
Informed Consent Forms (ICFs) and other patient-centric medical writing deliverables
Domain
Pharmaceutical / Clinical Research / Medical Writing
Required skills
Project management, budgeting, forecasting, resource management, risk evaluation, quality compliance monitoring, contract modification liaison, cross-functional collaboration, regulatory guideline knowledge
Preferred skills
Experience managing ICF content, pharmaceutical/CRO industry experience, medical writing experience (Regulatory/plain language)
Technologies
Tracking and management tools
Responsibilities
Develop project timelines, standards, budgets, forecasts and contract modifications; Collaborate with cross-functional team members to meet deliverables; Ensure achievement of final deliverables within contractual time periods; Evaluate and resolve risks to project quality, budget, or timeline; Ensure compliance with quality processes and requirements
Seniority
Senior, hands-on IC