Clinical Research Associate - Oncology - Detroit
Clinical Careers Page(22 days ago)
About this role
A Clinical Research Associate at ICON specializes in monitoring oncology clinical trials, ensuring compliance with regulations, and supporting site activities to facilitate successful study execution. The role involves collaboration with site staff, documentation, and tracking progress to meet project goals. The position offers regional travel opportunities and emphasizes diversity and well-being.
Required Skills
- Clinical Monitoring
- GCP
- CTMS
- eTMF
- Oncology
- Regulatory Compliance
- Patient Safety
- Data Entry
- Site Management
- Travel Coordination
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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