Job Summary
A company is looking for a Regulatory Coordinator for Thoracic Oncology.
Key Responsibilities
- Manage compliance and documentation for clinical trials, including IRB submissions and regulatory filings
- Coordinate study start-up activities and maintain communication with key stakeholders
- Prepare and maintain regulatory files and tracking databases to ensure audit readiness
Required Qualifications
- Bachelor's Degree or 1 year of relevant experience as an Associate Regulatory Coordinator
- 0-1 years of experience in a medical or scientific research setting preferred
- Fundamental knowledge of clinical trial conduct preferred
- Understanding of regulatory guidelines and the IRB submission process
- Proficiency in Microsoft applications and databases
Comments