Study Start Up Associate II
Clinical Careers Page(2 months ago)
About this role
A Study Start Up Associate II at ICON contributes to the preparation and readiness of clinical study sites and regulatory processes for trial initiation. The role sits within the clinical operations function supporting global clinical development programs and requires familiarity with clinical research standards and documentation. This position operates in a hybrid work model and collaborates with internal study teams and external site partners.
Required Skills
- ICH/GCP
- SOPs
- Regulatory Submissions
- Document Management
- TMF
- Quality Control
- Data Entry
- Translation Coordination
- Site Activation
- Forecasting
+4 more
Qualifications
- Bachelor's Degree (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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