Oncology Research Coordinator

Job Summary

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

Key Responsibilities

• Manages regulatory submissions and documentation for clinical trials, including consent and protocol amendments
• Liaises with various stakeholders on clinical trial regulatory operations and oversees timely submissions
• Coordinates audits and provides educational support to research staff on regulatory compliance

Required Qualifications, Training, and Education

• Bachelor's Degree with 1 year of clinical research experience, or a Master's Degree with 0-1 year of experience, or 3 years of relevant experience without a degree
• Health/Science degree preferred
• Previous experience in a healthcare setting, especially in cancer care or clinical research, is preferred
• Certification in clinical research (SoCRA, ACRP, RAPS, etc.) is preferred
• Regulatory knowledge of FDA/OHRP regulations is required