Oncology Research Regulatory Coordinator

Job Summary

A company is looking for a Coordinator - Oncology Research Regulatory Affairs & Compliance.

Key Responsibilities

• Manage regulatory submissions and documentation for clinical trial activities
• Liaise with various stakeholders on clinical trial regulatory operations
• Coordinate audits and ensure compliance with regulatory standards

Required Qualifications

• 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 clinical research 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
• Knowledge of FDA/OHRP regulations and complex regulatory processes is required