Parexel is on the lookout for a dedicated Clinical Research Associate (CRA) to join our team. In this exciting role, you will be responsible for the site management and monitoring of clinical trials, ensuring strict compliance with Good Clinical Practice (GCP) and regulatory standards.

Your expertise will be instrumental in working closely with investigator sites, fostering strong relationships, and enhancing the quality of trial execution. If you are passionate about oncology and clinical research, we encourage you to apply!

Key Responsibilities:
• Monitor clinical trial sites to ensure compliance with GCP and regulatory standards.
• Build and maintain effective working relationships with investigator sites.
• Manage the quality of trial execution efficiently and effectively.

Qualifications:
• Minimum of 3 years of experience in clinical research site monitoring, preferably in Oncology.
• Relevant bachelor’s degree.
• Fluent in English.
• Willingness to travel 60-80% of the time.

Join us in making a difference in the world of oncology!

Location: Trenton, New Jersey