Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and collection of requested records from physician offices for enrolled patients.
Scheduled Days / Hours: flex
2+ years research experience.
Education: High School Diploma or Equivalent required, Bachelor’s degree preferred and or nursing or oncology background.
Required License/Certifications/ Registration: CRA/ACRP preferred but not required.
Other Qualifications: Basic understanding of Microsoft Excel, Outlook and Word