Clinical Site Associate (In-House CRA)
Clinical Careers Page(29 days ago)
About this role
A Clinical Site Associate (In-House CRA) at ICON plc is a member of the clinical operations team who supports the conduct and quality of clinical trials at investigative sites. The role serves as a local liaison between sites and the broader study team, helping ensure studies are conducted in line with company and regulatory expectations.
Required Skills
- Site Management
- Document Management
- CTMS
- eTMF
- EDC
- Monitoring
- Regulatory Compliance
- Safety Reporting
- Data Entry
- Communication
+2 more
Qualifications
- Bachelor's Degree in 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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