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Piedmont Healthcare
Northlake, GA, United States
Clinical Research Coordinator
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Clinical Research Coordinator
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Description
Piedmont Healthcare is seeking a detail-oriented Clinical Research Coordinator to support clinical trials within the Scientific Research & Development department. In this role, you will coordinate study activities, including patient recruitment, informed consent, visit scheduling, data collection, and regulatory documentation to ensure compliance with GCP, IRB, and sponsor requirements. You will collaborate closely with investigators, clinicians, and patients to promote safety, data integrity, and patient-centered care. Piedmont offers a supportive, innovative culture with opportunities for ongoing training, professional growth, and advancement in healthcare research.Coordinate day-to-day operations of clinical research studies under PI supervision
Screen, recruit, and consent study participants in accordance with protocols and ethics standards
Collect, document, and enter clinical data into EDC systems ensuring accuracy and completeness
Schedule study visits, procedures, and follow-ups while maintaining study timelines
Prepare, maintain, and submit regulatory documents to IRB and sponsors
Monitor participant safety, report adverse events, and ensure protocol compliance
Collaborate with investigators, nurses, and sponsor/CRO teams to support study conduct
Maintain study files, source documents, and investigational product accountability
Participate in monitoring visits and audits, responding to findings and queries
Contribute to continuous process improvement and staff training within the research team
Clinical trial coordination
Good Clinical Practice (GCP) knowledge
Informed consent process
Electronic data capture (EDC) systems
Regulatory documentation (IRB/FDA)
Patient recruitment and screening
Source documentation and query resolution
Adverse event reporting
Clinical research budgeting and scheduling
Microsoft Office and EMR/EHR systems
Medical Insurance
Dental Insurance
Vision Insurance
Life Insurance
401k
Certified Clinical Research Coordinator (CCRC) preferred
Good Clinical Practice (GCP) training required or obtained within 6 months
CPR/BLS certification preferred
Job ID: f14adde5-5906099380
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Community Intel Unavailable
Details for Northlake, GA, United States are unavailable at this time.
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