ICF Manager
Clinical Careers Page(1 month ago)
About this role
A Medical Affairs Coordinator serving as an ICF Manager embedded within a pharmaceutical company, responsible for ownership of Master Informed Consent Forms for clinical trials. The role focuses on ensuring ICFs meet global regulatory standards, supporting study teams, and improving ICF workflows and turnaround times.
Required Skills
- ICF Development
- Protocol Interpretation
- Document Management
- Project Management
- Stakeholder Collaboration
- Regulatory Compliance
- Veeva
- Microsoft Office
- Communication
Qualifications
- Bachelor's Degree
- Life Sciences Preferred
- RN
- Master's Degree
- Doctorate
About Clinical Careers Page
iconplc.comICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.
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