Clinical Research Coordinator

Primary Responsibilities/Accountabilities:

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