Clinical Research Coordinator II: Lead Patient-Focused Trials

Intercoastal-Medical-Group; Sarasota (FL); On-site; USD 60,000 - 75,000; Full time

Job summary

Intercoastal Medical Group seeks a Clinical Research Coordinator II to manage day-to-day clinical trial activities in a healthcare setting. You will coordinate participant recruitment, consent processes, data collection, and regulatory compliance to ensure study integrity.

Responsibilities include collaboration with investigators, sponsors, and staff, as well as monitoring safety, maintaining documentation, and supporting quality improvement initiatives across studies.

Qualifications

• High School Diploma or Equivalent is required.
• Accredited Medical Assistant Program or Licensed Practical Nurse or Registered Nurse program completed.
• At least 3 years coordinating clinical research studies in healthcare/academic settings.
• Knowledge of FDA, IRB, and GCP regulations.
• Strong organizational and multi-study management abilities.
• Proficiency with electronic data capture systems and MS Office Suite.

Responsibilities

• Coordinate day-to-day activities of clinical research studies.
• Ensure compliance with study protocols, GCP, FDA and IRB guidelines.
• Maintain accurate study documentation (CRFs, regulatory binders, EDC).
• Collaborate with investigators, staff and sponsors to progress studies.
• Monitor participant safety and report adverse events per protocol.
• Schedule visits, collect samples, and perform required procedures.
• Assist in regulatory document preparation and submission.
• Train and mentor junior staff and support quality improvements.

Education

High School Diploma or Equivalent

Accredited Medical Assistant Program or Licensed Practical Nurse Program or Registered Nurse Program

3+ years coordinating clinical research studies

FDA/IRB/GCP knowledge

Strong organizational skills

Proficiency with electronic data capture systems

Microsoft Office Suite proficiency

Interpersonal and communication skills

Tools

Electronic Data Capture (EDC) systems

Microsoft Office

Job description

Intercoastal Medical Group seeks a Clinical Research Coordinator II to manage day-to-day clinical trial activities in a healthcare setting. You will coordinate participant recruitment, consent processes, data collection, and regulatory compliance to ensure study integrity.

Responsibilities include collaboration with investigators, sponsors, and staff, as well as monitoring safety, maintaining documentation, and supporting quality improvement initiatives across studies.