Study Delivery Specialist
Clinical Careers Page(2 months ago)
About this role
A Site Management Associate I at ICON plc is an early-career clinical research professional based in Poland supporting study delivery within a global contract research organization. The role sits within study delivery teams and contributes to operational governance, study lifecycle support, and cross-functional collaboration across phases and therapy areas.
Required Skills
- eTMF Management
- Study Tracking
- Vendor Management
- Budget Coordination
- Regulatory Knowledge
- GCP
- Risk Management
- Communication
- Project Coordination
- Time Management
Qualifications
- University Scientific Degree
- At Least Two Years Experience
- GCP
- ICH
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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