Clinical Research Coordinator (Contract)

Accelerated Clinical Trials; Snellville (GA); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

Hands-on experience

Professional development

Meaningful work

Job summary

Accelerated Clinical Trials is seeking a motivated Clinical Research Coordinator to support clinical trials from study start-up through closeout. The Coordinator will coordinate and implement protocols under the oversight of the Principal Investigator, ensure regulatory compliance, promote patient safety, and support high-quality study execution.

This contract role is based in Snellville, GA, and requires a Bachelor's degree in health sciences or related field, with clinical research experience

Qualifications

• Bachelor's degree in health sciences or related field.
• Clinical research experience preferred.
• Strong organizational, communication, and multitasking skills.
• Ability to work independently and as part of a team.

Responsibilities

• Maintain regulatory and study documentation
• Assist with study recruitment events
• Collect and enter study data; resolve queries in EDC systems
• Ensure compliance with GCP, IRB, and regulatory requirements
• Serve as liaison for sponsors, monitors, and internal departments

Education

Bachelor's degree in health sciences or related field

Job description

Clinical Research Coordinator (Contract)

Job Title: Clinical Research Coordinator (Contract)

Job Status: Full-time

Department: Clinical Research / Research Administration

Reports To: Clinical Research Manager

Job Summary

We're seeking a motivated Clinical Research Coordinator to support clinical trials from study start-up through closeout. The Clinical Research Coordinator is responsible for the coordination and implementation of clinical research protocols under the oversight of the Principal Investigator. This role ensures compliance with regulatory requirements, promotes patient safety, and supports high-quality study execution.

Key Responsibilities

• Maintain regulatory and study documentation
• Assist with study recruitment events
• Collect and enter study data; resolve queries in EDC systems
• Ensure compliance with GCP, IRB, and regulatory requirements
• Serve as liaison for sponsors, monitors, and internal departments

Qualifications

• Bachelor's degree in health sciences or related field
• Clinical research experience (preferred)
• Strong organizational, communication, and multitasking skills
• Ability to work independently and as part of a team

What We Offer

• Hands-on experience in clinical research and patient interaction
• Opportunities for professional development
• Meaningful work that supports patient care and scientific discovery