Study Delivery Specialist
Clinical Careers Page(29 days ago)
About this role
The Site Management Associate I (SMA I) at ICON is an entry-level role within the clinical study delivery organization. The role supports study delivery across clinical trial phases and contributes to maintaining the systems and processes that underpin study execution and regulatory readiness. The SMA I works closely with Study Delivery leads and cross-functional teams in a global clinical research environment.
Required Skills
- Study Coordination
- eTMF Oversight
- Systems Setup
- Tracking Tools
- Budget Coordination
- Vendor Management
- Risk Management
- Stakeholder Communication
- Regulatory Compliance
- GCP Knowledge
Qualifications
- University Life Science Degree
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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