Senior Clinical Research Coordinator - Trials & Site Ops

Syneos Health; Miami (FL); On-site; USD 55,000 - 85,000; Full time

Job summary

Illingworth Research Group in Miami seeks a Clinical Research Coordinator II to support multiple clinical trials, from site preparation to patient enrollment and data entry.

You will coordinate start-up activities, monitor patient safety, ensure regulatory compliance, and collaborate with investigators and sponsor teams to keep trials on track. The role requires strong organizational skills and the ability to manage schedules including evenings or weekends.

Qualifications

• Review protocols and documentation for accuracy and feasibility.
• Prepare and maintain TMF and site files.
• Coordinate regulatory and start-up activities.
• Support informed consent and data entry.

Responsibilities

• Review of assigned protocols and other protocol documentation (ICF, IB) for accuracy, feasibility, timing, and resources.
• Prepare and maintain the Investigator Site File and/ or Trial Master File (TMF) for the study.
• Participate in creation and review of timelines and start-up meetings (Investigator Meeting/SIV, Sponsor discussions, or other related meetings).
• Take the lead and/or overall coordination of all required start-up activities including, but not limited, to the following: Clinic logistics planning, schedule of clinic activities, and team training.

Job description

Illingworth Research Group in Miami seeks a Clinical Research Coordinator II to support multiple clinical trials, from site preparation to patient enrollment and data entry.

You will coordinate start-up activities, monitor patient safety, ensure regulatory compliance, and collaborate with investigators and sponsor teams to keep trials on track. The role requires strong organizational skills and the ability to manage schedules including evenings or weekends.