Sr. Clinical Research Associate
Clinical Careers Page(1 month ago)
About this role
A Senior Clinical Research Associate at ICON plc oversees and manages clinical trial activities to ensure they are conducted in accordance with protocols, regulatory requirements, and industry standards. The role supports data integrity and participant safety across multiple study sites and contributes to the overall success of clinical development programs.
Required Skills
- Site Monitoring
- Site Management
- Data Integrity
- GCP
- Clinical Software
- Training
- Stakeholder Management
- Communication
Qualifications
- Advanced Degree in 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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