Job Description

We are seeking a meticulous and experienced Clinical Research Associate (CRA) to join our clinical development team. In this role, you will be responsible for monitoring and managing clinical trials to ensure that they are conducted in compliance with regulatory requirements, company policies, and industry standards. You will work closely with the clinical team to assess trial progress, data collection, and patient safety.

Job Responsibilities

• Monitor the progress of clinical trials to ensure compliance with protocols, regulations, and Good Clinical Practice (GCP).
• Conduct site visits and ensure that clinical data is accurate, complete, and verifiable.
• Collaborate with investigators, study coordinators, and other team members to resolve issues and ensure that trials are running smoothly.
• Assist in preparing regulatory documentation and study reports.
• Ensure patient safety and data integrity are maintained throughout the trial process.