Study Delivery Specialist
Clinical Careers Page(1 month ago)
About this role
A Site Management Associate I (Study Delivery Specialist) at ICON supports the management and delivery of clinical trials by assisting with site-related activities, documentation, and administrative tasks. The role contributes to ensuring compliance with study protocols and regulatory standards while enabling efficient site operations. This is an entry-level position within the clinical operations function focused on supporting site teams and study delivery.
Required Skills
- Site Monitoring
- Regulatory Compliance
- GCP Knowledge
- Documentation
- Data Entry
- Communication
- Organization
- Recordkeeping
- Report Preparation
- Teamwork
Qualifications
- Bachelor's Degree in Life Sciences, Healthcare Administration, or Clinical Research
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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