About this role
We are seeking a Sponsor-Dedicated experience CRA with solid monitoring experience. Oncology expertise would be a plus. If you are eager to make an impact, this is your chance!
This role is for upcoming future opportunities that may arise at Fortrea
Key Responsibilities: In this role, you will
• Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements
• Build strong relationships with investigators and site staff
• Ensure high-quality data collection and patient safety
• Work closely with the sponsor, providing insights and updates on study prog