Clinical Study Coordinator
Clinical Careers Page(1 month ago)
About this role
ICON plc is a global healthcare intelligence and clinical research organization. The Clinical Study Coordinator based in Salt Lake City supports clinical research activities and contributes to the advancement of treatments and therapies within the clinical operations team.
Required Skills
- Clinical Trials
- Protocol Development
- Study Coordination
- Regulatory Compliance
- Data Monitoring
- Quality Control
- Project Management
- Communication
- Multitasking
- GCP
Qualifications
- Bachelor's Degree in Relevant Scientific Discipline
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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