Oncology Research Specialist

Job Summary

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

Key Responsibilities

• Assist with regulatory and compliance documentation for oncology research projects and clinical trials
• Compile, prepare, review, and submit protocol submissions throughout the study lifecycle
• Maintain documentation in an audit-ready manner and assist with site audits and inspections

Required Qualifications

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