Study Site Management Specialist
Clinical Careers Page(1 month ago)
About this role
A Site Activation Lead at ICON plc contributes to clinical development by supporting study start-up and aligning site and country distribution plans with client objectives. The role sits within ICON’s clinical research organization and works cross-functionally to support regulatory and quality-compliant study readiness.
Required Skills
- Site Activation
- Project Management
- Regulatory Knowledge
- Client Management
- Communication
- Timeline Management
- Study Planning
- Compliance
- Stakeholder Management
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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