RESEARCH COORDINATOR I

ATLANTA DIABETES ASSOCIATES PC • Atlanta, GA

just now • Onsite

About The Position

The Clinical Research Coordinator I will work within a leading endocrinology practice in Atlanta, GA, implementing, managing, and overseeing clinical studies related to diabetes and other endocrine disorders. The coordinator ensures compliance with ICH, GCP, and FDA standards and observes the guidelines set by Atlanta Diabetes Associates. Core responsibilities include patient recruitment, assisting with informed consent, monitoring study progress, and maintaining meticulous documentation for clinical trials. The role involves direct patient interaction, data entry, and managing study inventories. This in-office position may occasionally require evening or weekend hours, depending on project needs, and is ideal for those passionate about advancing endocrine research.

Requirements

• Prior experience in a medical office, laboratory, or research setting is preferred, with an emphasis on clinical research or endocrinology.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint) and general computer use.
• Understanding of human subject protection, Institutional Review Board (IRB) operations, and regulatory standards.
• Familiarity with medical and lab equipment and their protocols.
• Strong attention to detail, organizational skills, and ability to maintain confidentiality, particularly with HIPAA guidelines.
• Excellent interpersonal skills for effective communication with study participants, investigators, regulatory agencies, and the healthcare team.
• Adaptability and flexibility to handle changing responsibilities and environments, with the ability to work on multiple projects simultaneously.
• Commitment to professional growth, with access to ongoing training and development through workshops and seminars.

Responsibilities

• Implementing, managing, and overseeing clinical studies related to diabetes and other endocrine disorders.
• Ensuring compliance with ICH, GCP, and FDA standards and observing the guidelines set by Atlanta Diabetes Associates.
• Patient recruitment.
• Assisting with informed consent.
• Monitoring study progress.
• Maintaining meticulous documentation for clinical trials.
• Direct patient interaction.
• Data entry.
• Managing study inventories.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed