Clinical Research Associate

As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.

Key Responsibilities :

• Conduct site visits to monitor trial activities and ensure compliance with protocols and regulations.
• Collect, review, and manage clinical trial data to ensure accuracy and integrity.
• Oversee participant safety and adverse event reporting throughout the trial process.
• Establish and maintain relationships with clinical investigators and site staff.
• Assist in regulatory submissions and ensure documentation is complete and up-to-date.