Principal Study Start Up Associate
Clinical Careers Page(2 months ago)
About this role
A Principal Study Start Up Associate at ICON coordinates operational and strategic aspects of clinical trial submissions for countries in scope of the EU Clinical Trials Regulation. The role focuses on developing and driving EU CTR submission strategies, managing timelines and milestones, and ensuring timely, compliant submissions into the EMA CTIS in collaboration with central and country teams.
Required Skills
- Clinical Submissions
- EU CTR
- CTIS Portal
- Project Management
- Stakeholder Management
- Regulatory Knowledge
- Financial Tracking
- Virtual Teamwork
Qualifications
- BS 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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