CRA/ Sr CRA Denmark
Clinical Careers Page(1 month ago)
About this role
A Senior Clinical Research Associate at ICON plc oversees and manages clinical trial activities across multiple sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice. The role supports data integrity and participant safety throughout the study lifecycle and contributes to cross-functional trial execution.
Required Skills
- Monitoring
- Site Visits
- Data Integrity
- GCP
- Site Management
- Stakeholder Management
- Clinical Software
- Training
- Communication
- Problem Solving
+2 more
Qualifications
- Advanced Degree (Life Sciences/Nursing/Medicine)
- 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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