Informed Consent Manager
Amgen(5 days ago)
About this role
This role involves managing the development and quality of informed consent forms for clinical studies at Amgen, ensuring compliance with regulations and delivering high-quality materials to support global research operations. It emphasizes collaboration with various teams, process improvements, and incorporating patient feedback.
Required Skills
- Clinical Operations
- Regulatory Compliance
- Project Management
- Clinical Trial
- Content Editing
- Quality Assurance
- Global Coordination
- Patient Engagement
- Document Management
About Amgen
amgen.comAmgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics.
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