Clinical Trials Coordinator: Lead Study Operations

Green Key Resources; Florida; On-site; USD 50,000 - 70,000; Full time

Job summary

Green Key Resources seeks a Clinical Research Coordinator to support study execution in compliance with GCP, ICH, HIPAA and FDA regulations. You will screen patients, document data, collect vitals and assist with labs, ensuring timely reporting and coordination with the site team.

The role requires clinical experience or a Medical Assistant/LPN/EMT credential and may involve bilingual English/Spanish communication. Strong organizational skills are essential for success.

Qualifications

• Medical Assistant diploma, LPN/LVN, EMT credential or Associate’s degree required.
• Minimum 1 year of clinical research or clinical experience.
• Bi-lingual English/Spanish proficiency is a plus.

Responsibilities

• Screen patients for study enrollment and document sources clearly.
• Enter data in EDC and respond to queries promptly.
• Obtain vital signs and ECGs and assist with lab procedures as needed.
• Maintain logs, charts and study supplies; coordinate visits.
• Ensure HIPAA compliance and ALCOAC documentation practices.
• Support study start-up activities and attend site visits as required.

Skills

Clinical research

Bilingual English/Spanish

Strong organizational skills

Excellent communication

Education

Medical Assistant diploma

LPN/LVN credential

EMT credential

Associate’s degree

Tools

Microsoft Office

Electronic health records

Job description

Green Key Resources seeks a Clinical Research Coordinator to support study execution in compliance with GCP, ICH, HIPAA and FDA regulations. You will screen patients, document data, collect vitals and assist with labs, ensuring timely reporting and coordination with the site team.

The role requires clinical experience or a Medical Assistant/LPN/EMT credential and may involve bilingual English/Spanish communication. Strong organizational skills are essential for success.