Clinical Trials Coordinator - Impactful, Compliance-Driven

Evolution Research Group; Miami (FL); On-site; USD 52,000 - 78,000; Full time

Benefits offered by this job

Medical and dental coverage

401(k) matching

Paid time off

Job summary

Evolution Research Group is seeking a Clinical Research Coordinator to oversee coordination and management of clinical trials. You will distribute study medication, maintain confidential records, and ensure adherence to FDA regulations, GCP, ICH guidelines, and SOPs under the Site Director and Principal Investigator.

You will screen and enroll subjects, obtain informed consent, schedule visits, enter data, and report adverse events.

Qualifications

• Understand regulatory requirements, including GCP and ICH guidelines.
• Excellent interpersonal, written and verbal communication.
• Basic computer skills: Word, Excel, and study-related software.

Responsibilities

• Coordinate, organize, manage and implement clinical trials as required.
• Distribute study medication and instructions to research subjects under PI oversight.
• Maintain accurate, confidential trial documentation and files.
• Ensure compliance with protocol requirements under FDA regulations and SOPs.
• Screen, enroll subjects and schedule visits; obtain informed consent.
• Enter data and report adverse events per study protocol.
• Support site director and PI to ensure data integrity and subject safety.

Skills

Communication skills

Regulatory knowledge

Computer skills

Education

High School Diploma or equivalent

College degree preferred

Tools

Study Manager

Job description

Evolution Research Group is seeking a Clinical Research Coordinator to oversee coordination and management of clinical trials. You will distribute study medication, maintain confidential records, and ensure adherence to FDA regulations, GCP, ICH guidelines, and SOPs under the Site Director and Principal Investigator.

You will screen and enroll subjects, obtain informed consent, schedule visits, enter data, and report adverse events.