Set Up Specialist
Clinical Careers Page(5 days ago)
About this role
A Set Up Specialist at ICON coordinates the initial stages of clinical trials, ensuring all operational and logistical elements are in place for successful study execution. The role involves facilitating study setup processes and supporting compliance with regulatory standards to advance innovative treatments.
Required Skills
- clinical Trial
- Regulatory Submission
- GCP
- Site Management
- Documentation
- Study Coordination
- Biotech
- Healthcare Management
- Regulatory Compliance
- Logistics
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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