Study Start Up Associate II
Clinical Careers Page(1 month ago)
About this role
A Study Start Up Associate II at ICON supports initiation of clinical trials and ensures regulatory compliance for study start-up activities. The role contributes to advancing innovative treatments within a global clinical research organization and works closely with cross-functional teams to facilitate approvals and trial initiation.
Required Skills
- Regulatory Submissions
- Ethics Submissions
- Stakeholder Liaison
- Record Keeping
- Process Improvement
- Project Management
- Communication
- ICH-GCP
- Clinical Research
Qualifications
- Bachelor's Degree in Life Sciences
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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