Remote Clinical Research Coordinator I

Emory University; Atlanta (GA); Hybrid; USD 52,000 - 72,000; Full time

Job summary

Emory University seeks a Clinical Research Coordinator to manage administrative tasks in clinical trials and support study teams in Atlanta, GA. The role offers a flexible schedule with occasional remote work and requires residency in Georgia.

Responsibilities include data entry, patient recruitment support, attending study meetings, ordering supplies, reviewing records, phlebotomy as needed, and coordinating regulatory submissions.

Qualifications

• High School Diploma or GED with 3 years of admin support.
• Two years of college in a scientific, health related, or business program and 1 year admin support.
• Licensed practical nurse (LPN) with 1 year admin support or nursing experience.
• Bachelor's/Master's/MD/PhD in scientific/health related or business administration program.

Responsibilities

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

Skills

Administrative support

Data entry

Recruitment

Coordination

Documentation

Education

Bachelor's degree or higher in scientific/health/business field

Job description

Emory University seeks a Clinical Research Coordinator to manage administrative tasks in clinical trials and support study teams in Atlanta, GA. The role offers a flexible schedule with occasional remote work and requires residency in Georgia.

Responsibilities include data entry, patient recruitment support, attending study meetings, ordering supplies, reviewing records, phlebotomy as needed, and coordinating regulatory submissions.