Clinical Research Coordinator I: Start in Clinical Trials

Emory University; Atlanta (GA); On-site; USD 52,000 - 75,000; Full time

Job summary

Emory University is seeking a Clinical Research Coordinator to handle administrative tasks and support the conduct of clinical trials at an Emory location in Atlanta. You will manage data, assist in recruitment, coordinate study activities, and ensure regulatory compliance.

The role requires diverse qualifications, including data entry, patient recruitment, and knowledge of clinical procedures; remote work options are not stated and in-person presence is emphasized.

Qualifications

• High School Diploma or GED with three years of admin support experience.
• Or two years of college in scientific, health related, or business administration with one year admin support experience.
• Or licensed as an LPN with one year admin support or one year nursing experience.
• Or a Bachelor's/Master's/MD or PhD in a scientific, health related or business program.

Responsibilities

• Maintains data for 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 screens for recruitment of study participants.
• Collects study specimens according to protocol, including phlebotomy when needed.
• Coordinates services, schedules procedures, and tracks study charges.
• Assists with quality assurance and regulatory submissions.
• Performs related approved responsibilities as required.

Skills

Data entry

Patient recruitment

Study coordination

Records review

Phlebotomy

Quality assurance

Education

High School diploma or GED

Two years college in scientific/health or business administration

LPN license with admin experience

Bachelor's/Master/MD/PhD in scientific/health or business

Job description

Emory University is seeking a Clinical Research Coordinator to handle administrative tasks and support the conduct of clinical trials at an Emory location in Atlanta. You will manage data, assist in recruitment, coordinate study activities, and ensure regulatory compliance.

The role requires diverse qualifications, including data entry, patient recruitment, and knowledge of clinical procedures; remote work options are not stated and in-person presence is emphasized.