Join Prevail as a Clinical Research Associate specializing in oncology. In this contract position, you will oversee Phase I-IV clinical projects to ensure compliance and data integrity, performing monitoring activities both on-site and remotely.

As a Clinical Research Associate, you will be responsible for site management and monitoring of oncological studies. Your expertise will guide you in evaluating site performance, maintaining ICH-GCP compliance, and ensuring proper informed consent documentation. You'll play a crucial role in supporting subject recruitment and safety while effectively managing site-level communications and project timelines.

Key Responsibilities:
• Conduct site qualification, initiation, and monitoring visits
• Assess site performance and escalate serious issues
• Verify informed consent procedures and confidentiality measures
• Maintain accuracy of the Investigator Site File (ISF)
• Document activities in ...