Job Title: Clinical Research Coordinator

Work Location: Muscogee County, Georgia

Summary:

Seeking an experienced Clinical Research Coordinator to lead and develop a new research program at an expansion site. This role involves coordinating clinical trials, supporting site operations, and collaborating with multidisciplinary teams to ensure the success and growth of the research program.

Responsibilities:

• Lead the development and implementation of clinical research operations at a new site, establishing best practices and workflows.
• Coordinate all phases of clinical trials, including patient recruitment, screening, enrollment, and follow-up, ensuring adherence to study protocols.
• Serve as the primary contact for study sponsors, participants, and research stakeholders, providing timely updates and facilitating effective communication.
• Maintain accurate and up-to-date study documentation, regulatory binders, and patient records in compliance with GCP, ICH, and regulatory standards.
• Support daily site operations, ensuring compliance with regulatory requirements and optimizing research processes for efficiency and quality.
• Collect, verify, and manage clinical trial data, ensuring accuracy, completeness, and timely entry into electronic data capture systems.
• Identify and implement opportunities for process improvement to enhance research workflows and study performance.
• Work both independently and collaboratively with investigators, sponsors, and site staff to achieve study goals and support program growth.

Qualifications:

• Minimum of 5 years of experience as a research coordinator, preferably with mid-career experience or foreign-trained MD background.
• Clinical experience in cardiovascular medicine in a licensed role (e.g., RN, technologist, medical assistant, etc.).
• Bachelor’s degree in a relevant field (life sciences, healthcare, or clinical research) preferred.
• Minimum of 1–2 years of clinical research experience, including patient enrollment and study coordination.
• Strong communication skills and a positive, collaborative attitude.
• Ability to work independently and as part of a multidisciplinary team.
• Vision and initiative to grow and develop the research site.
• Strong organizational and time management skills, with attention to detail and quality.
• Clinical research certification (e.g., CCRP) preferred.
• Knowledge of GCP, ICH guidelines, and regulatory requirements.
• Experience with electronic data capture systems and regulatory documentation preferred.

Published Category: Clinical Operations & Development