Clinical Research Coordinator
Southeastern Clinical Research Institute, LLC
Richmond County, Gabon · Full Time
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- Experience
- Any
- Salary
- —
- Openings
- 1
- Posted
- 2 weeks ago
- Work mode
- In office
- Education
- Bachelor’s degree in a health-related field
- Eligibility
- Candidates with experience in research or clinical research operations are suitable, and applicants with a bachelor’s degree in a health-related field are preferred. Clinical research certification is an added benefit.
- Resume
- Required to apply
Job description
Company Overview
Southeastern Clinical Research Institute, LLC is an independent research site dedicated to advancing kidney disease care through the development of new therapies. The organization works with sponsors and partners to deliver dependable clinical research services and to support studies that can improve outcomes in nephrology. Its focus on quality, scientific rigor, and ethical research practices has established it as a respected name in kidney disease trials.
Role Summary
This full-time, on-site position is based in Augusta, GA, and centers on coordinating the daily activities of clinical trials. The Clinical Research Coordinator will support study execution by managing consent procedures, preparing source documentation, working across several digital systems each day, following assessment schedules, and keeping study records complete and up to date. The role involves close coordination with research staff, trial participants, sponsors, and regulatory bodies to help ensure studies are carried out smoothly, accurately, and in compliance with requirements.
Key Responsibilities
- Manage the day-to-day workflow of assigned clinical trials.
- Obtain and document informed consent from study participants.
- Prepare and maintain source documents and study records.
- Use multiple electronic platforms and systems as part of routine study operations.
- Track and follow the visit and assessment schedule for each protocol.
- Coordinate with research teams, participants, sponsors, and regulatory authorities.
- Support the ethical, accurate, and compliant conduct of clinical studies.
Qualifications
- Excellent organizational, communication, and people skills.
- Solid grasp of clinical protocols and how they are carried out in practice.
- Background in research and clinical research operations.
- Understanding of how clinical trials are structured and run.
- Ability to work within ethical, regulatory, and institutional compliance requirements.
- Strong multitasking and prioritization skills in a clinical environment.
- A bachelor’s degree in a health-related discipline is preferred.
- Clinical research certifications are considered an added advantage.
Additional Information
This is an onsite role in Augusta, Georgia. No salary, openings, start date, or application deadline were specified in the source information.