Clinical Research Coordinator

l research more efficient and accessible. They focus on on large-volume recruitment and retention of diverse and specialty patient populations, and have an experienced team with extensive physician partnerships help deliver high-quality data across a wide range of therapeutic areas!

The Role:

We are seeking an temporary CRC to support the site for 3 - 4 months. There is eligibility for a permanent role based on site needs and performance
• Coordinate all aspects of assigned clinical trials
• Conduct subject visits and ensure accurate, timely documentation in compliance with all applicable standards
• Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
• Manage subject recruitment, informed consent, and retention activities (There is a recruitment team to support day to day recruitment)
• Ensure timely EDC data entry and resolution of queries
• Report and follow up on AEs, SAEs, and protocol deviations
• Collaborate with investigators, sponsors/CROs, labs, and internal teams
• Prepare for and participate in monitoring visits, audits, and inspections
• Maintain regulatory documentation and ensure training compliance for amendments and systems
• Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)
• Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory

Requirements:
• 1+ years exp as a Research Assistant or CRC on sponsor backed trials
• Ability to work on site M-F (NO hybrid or remote days)
• Ok with a 3 month employment term to start