A company is looking for a Clinical Research Associate (CRA).
Key Responsibilities
Assist with study planning, execution, and investigator site management
Write and assemble regulatory submissions, draft study protocols and reports
Monitor investigational sites for protocol adherence and oversee patient enrollment
Required Qualifications
5+ years of clinical research monitoring experience
Bachelor's degree in Life Sciences
Strong knowledge of ICH GCP, FDA, and IRB requirements
Experience in independent site monitoring and management
Leadership experience, including mentoring junior CRAs
Clinical Research Associate • Riverside, California, United States
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