Join Parexel as a Clinical Research Associate (CRA) II and play a crucial role in the management and monitoring of clinical trials focused on ensuring quality and patient safety. As a key member of our team, you will engage with investigator sites and resolve protocol-related issues effectively.

Key Responsibilities:
• Manage and monitor clinical trials, ensuring adherence to protocols and regulatory requirements.
• Foster strong relationships with investigator sites through effective communication and support.
• Identify and resolve issues related to studies to maintain high standards of quality and compliance.

Qualifications:
• Bachelor's degree in life sciences or a related field.
• A minimum of 3 years of monitoring experience in clinical research, with a preference for oncology experience.
• Willingness and ability to travel extensively (60-80%).

Be part of Parexel’s mission to advance clinical trials and make a significant impact in oncology. We look forward to your application!