Site & Study Start Up Specialist
Clinical Careers Page(24 days ago)
About this role
A Study Start Up Associate II at ICON supports the initiation of clinical trials by managing regulatory submissions and ensuring compliance with applicable guidelines. The role works with cross-functional stakeholders to obtain approvals, maintain study documentation, and help streamline study start-up processes.
Required Skills
- Regulatory Submissions
- Stakeholder Liaison
- Documentation
- ICH-GCP
- Project Management
- Communication
- Process Improvement
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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