Study Start up Associate II - Regulatory
Clinical Careers Page(12 days ago)
About this role
ICON plc is a global healthcare organization focused on clinical research. The company seeks a Study Start Up Associate II to drive the initiation of clinical trials by managing regulatory submissions, coordinating with teams, and supporting compliance and process improvements in a flexible, home or office-based setting.
Required Skills
- Regulatory Submissions
- Clinical Research
- Project Management
- ICH-GCP
- Regulatory Affairs
- Documentation
- Communication
- Stakeholder Management
- Languages
- Process Improvement
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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