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 research role supporting the readiness and regulatory compliance of clinical trial sites. Based in Arden Hills, MN, the role works cross-functionally with internal teams and external clinical sites to enable successful participation in studies. It contributes to overall clinical development delivery within a global healthcare organization.
Required Skills
- IRB Submissions
- ICF Negotiation
- Regulatory Documents
- Site Start Up
- eTMF
- CTMS
- Site Management
- Communication
- Multi-Tasking
- Customer Service
+2 more
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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