Clinical Research Coordinator

Job Summary
We are seeking an experienced Clinical Research Coordinator in our Lawrenceville, GA Nephrology Research office to join our team and drive forward innovative clinical trials that impact patient care and medical advancements. In this vital role, you will coordinate all aspects of clinical research studies, ensuring compliance with regulatory standards, managing data collection, and supporting the overall success of our research initiatives. Your energetic approach will help facilitate smooth operations, foster collaboration with multidisciplinary teams, and uphold the highest standards of clinical excellence. This paid position offers an exciting opportunity to contribute meaningfully to groundbreaking research while developing your expertise in clinical development.

Experience in the conduct of Nephrology trials is preferred, but not required.

$30/hr, negotiable depending on experience.

Must currently live in the Atlanta area.

Responsibilities

• Oversee the planning, organization, and execution of clinical trials in accordance with FDA regulations and ICH Good Clinical Practice (GCP) guidelines.
• Manage participant recruitment, screening, enrollment, and ongoing monitoring to ensure safety and protocol adherence.
• Review and verify all study documentation for accuracy, completeness, and regulatory compliance.
• Collect, manage, and analyze data using electronic medical record (EMR) systems and statistical software to support research objectives.
• Conduct patient assessments including vital signs, blood sampling (phlebotomy), and monitoring of clinical laboratory results.
• Ensure compliance with HIPAA regulations to protect patient privacy and confidentiality throughout all study activities.
• Supervise research staff and coordinate with multidisciplinary teams to facilitate seamless trial operations.

Skills

• Extensive knowledge of clinical trials management, including patient monitoring and data collection procedures.
• Strong understanding of medical terminology, blood sampling techniques, and clinical laboratory processes.
• Proficiency with EMR systems.
• Familiarity with FDA regulations and ICH GCP standards. .
• Experience in clinical development processes from Study Start-up to Close-out.
• Knowledge of phlebotomy techniques, blood sampling procedures, ECG and vital signs measurement is required.
• Ability to review complex documentation meticulously while maintaining attention to detail in a fast-paced environment.

Pay: $30.00 per hour

Expected hours: 40 per week

Benefits:

• Dental insurance
• Health insurance
• Paid time off

Work Location: In person