What are the responsibilities and job description for the Clinical Research Coordinator position at Equity Medical?
Company Description
Equity Medical is an integrated clinical research site network conducting Phase I–IV clinical trials across multiple therapeutic areas. With five research sites in New York, Kentucky, and Tennessee, we combine experienced investigators, strong operational expertise, and advanced recruitment capabilities to deliver high-quality clinical research. Our work focuses on expanding trial access for diverse and underrepresented populations, supported by a dedicated quality assurance division committed to data integrity, regulatory compliance, and audit readiness.
Role Description
We are seeking a full-time Clinical Research Coordinator to join our team onsite in Memphis, Tennessee. In this role, you will coordinate day-to-day clinical trial activities, support study participants, and work closely with investigators and research staff to ensure studies are conducted according to protocols, Good Clinical Practice (GCP), and applicable regulatory requirements.
Key Responsibilities
- Coordinate participant screening, enrollment, study visits, and follow-up activities.
- Support the informed consent process in accordance with study requirements and delegated responsibilities.
- Maintain accurate, complete, and timely source documentation and study records.
- Collect and enter study data, resolve queries, and track study timelines.
- Collaborate with investigators, sponsors, and study monitors to support study execution and monitoring visits.
- Assist with regulatory documentation and compliance with site standard operating procedures.
- Support participant recruitment and retention while protecting participant confidentiality.
Qualifications
- Previous clinical research experience; Clinical Research Coordinator experience preferred.
- Knowledge of GCP, ICH guidelines, informed consent, and applicable regulatory requirements.
- Strong organizational skills, attention to detail, and the ability to manage competing priorities.
- Excellent communication skills and a participant-centered approach.
- Experience with electronic data capture systems and electronic study documentation.
- Experience working with diverse and underserved populations preferred.
- Bachelor’s degree in a health science, life science, or related field preferred; equivalent relevant experience will be considered.
- Ability to work onsite in Memphis, Tennessee.