ICF Manager

Job Summary

A company is looking for an ICF Manager.

Key Responsibilities

• Develop and manage Master Informed Consent Forms (ICFs) for clinical trials
• Coordinate ICF reviews and revisions, ensuring compliance with regulatory requirements
• Serve as a Subject Matter Expert (SME) in ICF development and process optimization

Required Qualifications, Training, and Education

• Bachelor's Degree or international equivalent required; Life Sciences preferred
• 4+ years of experience in the pharmaceutical industry and/or clinical research organization
• 2+ years of experience in study start-up and ICF development
• Knowledge of global regulatory and compliance requirements for clinical research
• Experience with drafting and managing ICF processes at site and CRO/sponsor levels