Nurse Coordinator

Ladgov Corporation; Atlanta (GA); On-site; USD 60,000 - 80,000; Part time

Job summary

Ladgov Corporation is seeking a Research Nurse Coordinator to assist with clinical trials at Emory University Hospital & Emory Midtown Hospital in Atlanta, GA. Responsibilities include screening candidates, collecting clinical trial data, and ensuring regulatory compliance. Applicants must hold an active RN license, have clinical research coordination experience, and possess strong organizational and communication skills. The role is part-time, approximately 20 hours per week.

Qualifications

• 2–3 years of clinical research coordination or equivalent clinical trial experience.
• Strong knowledge of FDA regulations, Good Clinical Practice (GCP), and IRB processes.
• Excellent organizational and documentation skills with ability to maintain audit‑ready records.

Responsibilities

• Screen candidates for clinical trials by reviewing medical records.
• Collect, enter, and maintain clinical trial data.
• Prepare for and support monitoring visits, ensuring data completeness.

Skills

Clinical research coordination

Organizational skills

Communication skills

Education

Active, unrestricted Registered Nurse (RN) license

Tools

Electronic data capture systems

Job description

Position: Research Nurse Coordinator
Location: Emory University Hospital & Emory Midtown Hospital, Atlanta, GA
Schedule: ~20 hours per week

Key Responsibilities:

Screen candidates for clinical trials by reviewing medical records and ensuring protocol-required testing is completed.

Collect, enter, and maintain clinical trial data in binders and electronic databases; attend procedures to capture non-standard‑of‑care data.

Upload imaging files for review and troubleshoot transmission errors.

Prepare for and support monitoring visits, ensuring data completeness, accuracy, and audit‑readiness.

Document and report adverse events, including coordinating with outside medical facilities for records.

Qualifications:

Active, unrestricted Registered Nurse (RN) license.

2–3 years of clinical research coordination or equivalent clinical trial experience.

Strong knowledge of FDA regulations, Good Clinical Practice (GCP), and IRB processes.

Proficiency with electronic data capture systems and medical record documentation.

Excellent organizational and documentation skills with ability to maintain audit‑ready records.

Strong communication and interpersonal skills for working with investigators, monitors, and clinical staff.