Clinical Research Associate - Remote

Overview

The Clinical Research Associate (CRA) will be responsible for monitoring clinical trials to ensure compliance with regulatory requirements and study protocols.

In Short

• Conduct site visits including initiation, monitoring, and close-out.
• Monitor patient safety and data integrity.
• Ensure compliance with Good Documentation Practices.
• Manage multiple protocols across different therapeutic areas.
• Provide training and support to site staff.
• Review case report forms for accuracy.
• Maintain communication with investigators and sponsors.
• Assist in resolving site-specific issues.
• Support ethics submissions and regulatory documentation.
• Contribute to process improvement and adherence to SOPs.

Requirements

• Minimum of 2 years’ independent monitoring experience.
• Strong understanding of ICH-GCP and regulatory guidelines.
• Experience in sponsor-dedicated and multi-sponsor settings preferred.
• Ability to manage multiple sites and protocols.
• Excellent communication and problem-solving skills.
• Ability to travel for site visits.
• Degree in Life Sciences, Pharmacy, Nursing, or related field.

Benefits

• Opportunities for professional development.
• Collaborative work environment.
• Exposure to various therapeutic areas.