Clinical Site Associate
Clinical Careers Page(1 month ago)
About this role
A Clinical Site Associate at ICON plc is a clinical research professional supporting clinical trial operations within a global healthcare intelligence and research organization. The role contributes to ensuring high-quality trial conduct and regulatory compliance across study sites while collaborating with cross-functional teams to support study deliverables.
Required Skills
- Site Management
- Document Management
- TMF
- CTMS
- eTMF
- Data Entry
- Audit Readiness
- GCP
- Communication
- Organization
+3 more
Qualifications
- Bachelor's Degree (Life Sciences or Healthcare)
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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