Join CMRG as a Clinical Research Associate, focusing on data accuracy and regulatory compliance in oncology research. This full-time position supports crucial clinical trial operations.
As a key member of the clinical research team, you will manage the oversight of CMRG-sponsored studies, ensuring compliance with regulatory requirements. You will be involved in creating protocols, managing submissions, and monitoring trial progress. Your attention to detail and regulatory knowledge will be vital to uphold high standards in research.
Key Responsibilities:
• Support regulatory submission processes and amendments
• Ensure trial compliance with regulatory bodies
• Coordinate monitoring for oncology clinical trials
• Conduct data cleaning and maintain databases
• Communicate effectively with stakeholders across trials
Requirements:
• Bachelor of Science degree or equivalent qualification
• 2+ years’ experience in clinical research
• Proficient in both Englis...