Oncology Research Specialist

Job Summary

A company is looking for an Oncology Research Specialist - Regulatory Affairs & Compliance.

Key Responsibilities

• Assists with regulatory and compliance documentation for oncology research projects and clinical trials
• Compiles, prepares, reviews, and submits protocol submissions from study start-up through termination
• Maintains documentation for assigned studies in an audit-ready manner and serves as a liaison to the IRB

Required Qualifications, Training, and Education

• High School Diploma or GED required; bachelor's degree preferred in Health/Science
• Experience in a healthcare setting preferred, especially in cancer care and/or clinical research
• Certification in clinical research (SoCRA, ACRP, RAPS, etc.) preferred
• Must reside in the Greater Charlotte area due to possible on-site requirements
• Must speak and write clearly in English