Clinical Research Associate (Start Up) - Oncology - Los Angeles, CA
Clinical Careers Page(22 days ago)
About this role
The role involves managing and supporting clinical trial site activation and start-up processes in the pharmaceutical industry, with a focus on oncology trials. The position requires coordination with various stakeholders, ensuring regulatory compliance, and maintaining documentation for successful study initiation.
Required Skills
- GCP
- ICH Guidelines
- Site Monitoring
- Regulatory Compliance
- Clinical Trials
- CTMS
- EDC
- eTMF
- Risk-Based Monitoring
- Patient Recruitment
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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