Onsite Memphis CRC - Patient-Centric Trials

Equity Medical LLC.; Memphis (TN); On-site; USD 52,000 - 75,000; Full time

Job summary

Equity Medical is seeking a full-time Clinical Research Coordinator to work onsite in Memphis, Tennessee. You will coordinate day-to-day clinical trial activities, support participants, and ensure studies follow protocols, GCP, and regulatory requirements.

Responsibilities include screening/enrollment, informed consent, data entry, and collaboration with investigators, sponsors, and monitors. Experience with EDC systems and diverse populations is preferred.

Qualifications

• Clinical research experience; Coordinator experience preferred.
• GCP/ICH guidelines and regulatory requirements knowledge.
• Strong organization, attention to detail, and prioritization.

Responsibilities

• Coordinate participant screening, enrollment, visits, and follow-up.
• Support informed consent processes per study requirements.
• Maintain source documentation and study records.
• Collect and enter data, resolve queries, and track timelines.
• Collaborate with investigators, sponsors, and monitors.
• Assist with regulatory documentation and SOP compliance.
• Support recruitment and retention while protecting confidentiality.

Skills

Strong organizational skills

Attention to detail

Excellent communication skills

Participant-centered approach

Ability to manage competing priorities

Education

Bachelor’s degree in health science or life science

Tools

Electronic data capture (EDC) systems

Job description

Equity Medical is seeking a full-time Clinical Research Coordinator to work onsite in Memphis, Tennessee. You will coordinate day-to-day clinical trial activities, support participants, and ensure studies follow protocols, GCP, and regulatory requirements.

Responsibilities include screening/enrollment, informed consent, data entry, and collaboration with investigators, sponsors, and monitors. Experience with EDC systems and diverse populations is preferred.