TALENT Software Services

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**
  • Seniority level

    Mid-Senior level
  • Employment type

    Full-time
  • Job function

    Research, Analyst, and Information Technology
  • Industries

    IT Services and IT Consulting, Software Development, and Financial Services

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