Clinical Research Coordinator II: Drive Patient-Centric Trials

ADP, Inc.; Sarasota (FL); On-site; USD 46,000 - 75,000; Full time

Job summary

Intercoastal Medical Group in Sarasota, FL is seeking a Clinical Research Coordinator II to manage clinical trials and ensure regulatory compliance across studies. You will coordinate participant recruitment, informed consent, data collection, and study operations while liaising with investigators, sponsors, and regulatory bodies to maintain study integrity.

The role emphasizes adherence to GCP and FDA guidelines, with salary commensurate with experience, and opportunities to contribute to

Qualifications

• Minimum: high school diploma or equivalent.
• Completion of accredited medical assistant, LPN, or RN program.
• At least 3 years coordinating clinical research in healthcare or academic setting.
• Knowledge of FDA, IRB, and GCP regulations.

Responsibilities

• Coordinate day-to-day clinical study activities including recruitment and follow-up.
• Ensure compliance with study protocols and regulatory requirements.
• Maintain accurate study documentation and regulatory binders.
• Collaborate with investigators, staff, and sponsors to progress studies.
• Monitor participant safety and report adverse events.
• Schedule visits, collect samples, and perform protocol procedures.
• Prepare regulatory documents and study reports.
• Train and mentor junior staff and support quality initiatives.

Skills

Strong organizational skills

Communication skills

Attention to detail

Problem-solving

Interpersonal collaboration

Education

High School Diploma or Equivalent

Accredited medical assistant / LPN / RN program

Tools

Electronic Data Capture (EDC) systems

Microsoft Office Suite

Job description

Intercoastal Medical Group in Sarasota, FL is seeking a Clinical Research Coordinator II to manage clinical trials and ensure regulatory compliance across studies. You will coordinate participant recruitment, informed consent, data collection, and study operations while liaising with investigators, sponsors, and regulatory bodies to maintain study integrity.

The role emphasizes adherence to GCP and FDA guidelines, with salary commensurate with experience, and opportunities to contribute to