Job Details

A company is looking for an Oncology Research Specialist - Regulatory Affairs & Compliance.Key ResponsibilitiesAssists with regulatory and compliance documentation for oncology research projects and clinical trialsCompiles, prepares, reviews, and submits protocol submissions from study start-up through terminationMaintains documentation for assigned studies in an audit-ready manner and serves as a liaison to the IRBRequired Qualifications, Training, and EducationHigh School Diploma or GED required; bachelor's degree preferred in Health/ScienceExperience in a healthcare setting preferred, especially in cancer care and/or clinical researchCertification in clinical research (SoCRA, ACRP, RAPS, etc.) preferredMust reside in the Greater Charlotte area due to possible on-site requirementsMust speak and write clearly in English