Clinical Research Coordinator I — Study Ops & Data

Socket.dev; Atlanta (GA); On-site; USD 52,000 - 72,000; Full time

Job summary

Emory University in Atlanta, GA is seeking a Clinical Research Coordinator to support the conduct of clinical trials. You will manage data, source documents, and assist with participant recruitment, study visits, and regulatory tracking.

The role involves coordinating schedules, reviewing medical records, collecting specimens, and ensuring QA and compliance while collaborating with study teams across departments.

Qualifications

• High School Diploma or GED with 3 years admin support experience.
• Alternatively, 2 years of college in science/health/business and 1 year admin support.
• Or LPN license with 1 year admin support or 1 year LPN experience.
• Or Bachelor's/Master/MD/PhD in a scientific, health-related or business administration program.

Responsibilities

• Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
• Assists with patient recruitment.
• Attends study meetings.
• Orders and maintains equipment and supplies.
• Reviews medical records and conducts screenings for recruitment of study participants.
• Collects study specimens according to protocol and prepares for shipping.
• Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges.
• Assists with quality assurance and tracks regulatory submissions.
• Performs related approved responsibilities as required.

Skills

Administrative support

Data entry

Patient recruitment

Scheduling

Quality assurance

Education

High School Diploma or GED

Two years of college in scientific/health/business

Licensed Practical Nurse (LPN)

Bachelor's degree

Master's degree

MD or PhD

Job description

Emory University in Atlanta, GA is seeking a Clinical Research Coordinator to support the conduct of clinical trials. You will manage data, source documents, and assist with participant recruitment, study visits, and regulatory tracking.

The role involves coordinating schedules, reviewing medical records, collecting specimens, and ensuring QA and compliance while collaborating with study teams across departments.