Informed Consent Manager

Job Summary

A company is looking for an Informed Consent Manager to support global clinical studies by delivering high-quality informed consent forms.

Key Responsibilities

• Manage the end-to-end delivery of study-specific informed consent forms (ICFs), ensuring quality and compliance
• Review and edit ICF content to align with study protocols and regulatory requirements
• Coordinate ICF translations and maintain tracking, reconciliation, and status reporting across studies

Required Qualifications

• Pharmaceutical and clinical trial processes expertise
• Experience in a global team structure and project management
• Doctorate degree or equivalent experience in clinical trials
• 5 years' work experience in life sciences or a medically related field
• Experience in clinical trial operations or authoring ICF forms preferred