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Clinical Research Coordinator

Company: Medix
Location: Pasadena
Posted on: November 10, 2018

Job Description:

Clinical Research CoordinatorDescription:A great opportunity to join a growing research facility!Job Details:

  • Review new protocols and attend research meetings to give input on financial and clinical feasibility
  • Help implement new protocols and assign new projects to appropriate departments
  • Help with IRB submissions, review, and approval
  • Help with determining appropriate research budgets
  • Help maintain inventory of required study supplies
  • Develop system for data collection for new trials
  • Act as a point of contact for study sponsors
  • Screen patients for trial eligibility
  • Informed Consent coordination
  • Managing research subject on assigned clinical trials (scheduling, protocol adherence, collecting samples)
  • Reporting of SAEs
  • Help with regulatory documentation and coordination
  • Complete Case Report Forms
  • In charge of research billing compliance
  • Coordinator monitor visits
  • Submit invoices for patient care charged funded by research studies
  • Help with final IRB report
  • Ensure all study documents are complete in accordance with all regulatory standards
  • Assist with some data analysis
  • Utilize and be familiar with EDC systems
  • Team player
  • Maintain current knowledge with department functions and regulatory guidelines
  • Maintain patient and study confidentialityJob Requirements
    • Bachelors Degree
    • 2-5 years of research experience preferredJob RequirementsBachelors Degree2-5 years of research experience preferred

      Keywords: Medix, Pasadena , Clinical Research Coordinator, Healthcare , Pasadena, California

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