Sr Clinical Research Coordinator

CAREERXCHANGE, Inc.; Miami (FL); On-site; USD 44,083 - 59,236; Part time

Job summary

CAREERXCHANGE, Inc. is looking for an experienced Senior Clinical Research Coordinator in Miami, FL. This role is a 15-week contract focused on managing clinical research studies and ensuring compliance with regulatory requirements while providing exceptional patient care.

Applicants should have a minimum of 3 years of experience in clinical research coordination and possess strong knowledge of GCP. The position offers a pay range of $32.00 to $43.00 per hour, with a schedule from Monday to Friday.

Qualifications

• Minimum 3 years of clinical research coordination experience.
• Experience with industry-sponsored clinical trials.
• Strong organizational and communication skills.

Responsibilities

• Coordinate and manage clinical research studies.
• Screen, recruit, and consent study participants.
• Ensure compliance with GCP and FDA regulations.
• Prepare for audits and sponsor visits.

Skills

Clinical research coordination experience

Knowledge of GCP

FDA regulations

Excellent communication skills

Multitasking skills

Tools

Electronic medical records (EMR)

Clinical trial management systems

Job description

Location

Miami, FL; Job Type: Contract (15 Weeks); Schedule: Monday – Friday, 8:30 AM – 5:00 PM; Pay: $32.00 – $43.00 per hour.

Job Summary

We are seeking an experienced Senior Clinical Research Coordinator to support a busy clinical research team during a 15-week contract assignment. This role is responsible for coordinating all aspects of clinical research studies, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines while delivering exceptional patient care.

Responsibilities

• Coordinate and manage multiple clinical research studies from start-up through closeout.
• Screen, recruit, consent, and schedule study participants.
• Collect, document, and maintain accurate study data and source documentation.
• Ensure compliance with FDA, IRB, GCP, and sponsor requirements.
• Prepare for sponsor visits, monitoring visits, and audits.
• Coordinate study procedures, laboratory specimens, and investigational product accountability.
• Maintain regulatory binders and study documentation.
• Communicate effectively with investigators, sponsors, research staff, and participants.
• Assist with data entry, query resolution, and timely reporting of adverse events.

Qualifications

• 3+ years of clinical research coordination experience required.
• Experience coordinating industry-sponsored clinical trials.
• Strong knowledge of GCP, FDA regulations, and IRB processes.
• Excellent organizational, communication, and multitasking skills.
• Proficiency with electronic medical records (EMR) and clinical trial management systems is preferred.
• Current CPR certification and Clinical Research certification (CCRC or CCRP) are a plus.

CAREERXCHANGE, INC is an EOE.