Senior Clinical Research Associate
Clinical Careers Page(14 days ago)
About this role
ICON plc is seeking a Senior Clinical Research Associate to oversee clinical trial activities, ensuring compliance with regulations, data integrity, and participant safety. The role involves monitoring trial sites, collaborating with teams, and providing training to site staff. It requires managing multiple projects and maintaining strong stakeholder relationships.
Required Skills
- GCP
- Clinical Trial Management
- Monitoring
- Site Management
- CTMS
- Data Verification
- Regulatory Compliance
- On-site Monitoring
- Source Data Verification
- Investigation Product
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.
View more jobs at Clinical Careers Page →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Clinical Careers Page
Similar Jobs
Clinical Research Associate II
Fortrea(3 months ago)
FSP CRA II (Beijing)
Fortrea(24 days ago)
Clinical Trial Manager (FSO)
Clinical Careers Page(17 days ago)
Clinical Research Associate I - Sponsor dedicated - Based in Hungary
Clinical Careers Page(6 days ago)
FSP CRA(Tianjin)
Fortrea(1 month ago)
Clinical Research Associate II
Fortrea(1 month ago)