Sr. Clinical Research Associate
Clinical Careers Page(1 month ago)
About this role
A Senior Clinical Research Associate at ICON Plc oversees clinical trial conduct across study sites to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice. The role focuses on protecting participant safety and ensuring data integrity throughout the study lifecycle. The position supports study success through collaboration with cross-functional teams and site stakeholders.
Required Skills
- Clinical Monitoring
- Site Management
- GCP
- Data Integrity
- Clinical Software
- Stakeholder Management
- Training
- Communication
- Travel
Qualifications
- Advanced Degree (Life Sciences, Nursing, or Medicine)
- Valid Driver's License
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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