As a Clinical Research Associate, you will monitor clinical trials, ensuring that investigators adhere to the study protocol and regulatory requirements. You will act as the liaison between the study sponsor and the clinical research site to guarantee quality data and patient safety.

The Regulatory Affairs Specialist will oversee submissions to health authorities and ensure compliance with local and international regulations. You’ll be responsible for preparing and maintaining regulatory documentation for clinical trials and drug approvals.

The Data Analyst will manage and analyze data from clinical trials, ensuring accurate and actionable insights for research teams. Your role includes creating reports, maintaining databases, and ensuring data integrity throughout the trial process.