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Clinical Research Coordinator
1 month ago
Screening and recruitment of potential patients for protocol eligibility.
Scheduling patients and maintain consent forms and case reports.
Data collection and reporting for sponsors and regulatory bodies
Coordinate internal and external audits
Submit adverse events, protocol deviations, and safety letters according to local/federal guidelines
Identify and participate in quality improvement opportunities
Qualifications:
BCLS certified from AHA or ARC
3 years of clinical research experience
Preferred:
6–12 months Oncology experience
SoCRA or ACRP certification
Phlebotomy certification
MA diploma from DAPIP accredited program or LVN licensed in CA
Serve as lead coordinator on a portfolio of Chemo/Onc research studies
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