Study Start Up Associate II - Medical Device - Arden Hills, MN
Clinical Careers Page(1 month ago)
About this role
The Study Start Up Associate II at ICON is a mid-level clinical operations role supporting medical device clinical trials at the Arden Hills, MN campus. The position focuses on coordinating site start-up processes and ensuring regulatory and policy compliance to enable successful study participation and progression.
Required Skills
- IRB Submissions
- ICF Customization
- Regulatory Documentation
- Document Management
- Site Start-Up
- CTMS
- eTMF
- Communication
- GCP Compliance
- Time Management
Qualifications
- Bachelor's Degree
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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