Clinical Research Coordinator I: Accelerate Trials & Care

Iterative Health; Memphis (TN); On-site; USD 52,000 - 75,000; Full time

Job summary

Iterative Health seeks a CRC I to support day‑to‑day clinical trial activities and ensure patient safety and protocol compliance. You will coordinate patient visits, collect data, and assist with regulatory requirements across GI, hepatology, obesity, and cardiology studies.

Ideal candidates have 1–3 years in clinical research or healthcare, are detail-oriented, and can manage competing priorities in a fast-paced environment while fostering strong teamwork with sponsors, CROs, and site staff.

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required.
• 1–3 years of clinical research or healthcare experience required.
• Must be able to perform blood draw, medical review (blood pressure, height, weight etc.) & EKGs.
• Strong organizational skills and attention to detail.
• Ability to manage competing priorities in a fast-paced environment.
• Ability to read, interpret, and apply research protocols and clinic policies.
• Proficiency with standard office software and willingness to learn clinical research systems.
• Familiarity with CTMS or EDC systems preferred.

Responsibilities

• Support the coordination and execution of industry-sponsored clinical trials under the guidance of site leadership and senior research staff.
• Coordinate patient visits, procedures, and study-related activities in accordance with protocol requirements and study timelines.
• Support patient recruitment and retention activities including chart review, patient outreach, scheduling, and informed consent coordination.
• Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs.
• Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, and investigational product accountability, as permitted by applicable regulations, training, and organizational policy.
• Maintain accurate and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms.
• Ensure high-quality data entry and support timely resolution of data queries.
• Serve as a point of contact for study participants throughout study participation.
• Maintain ongoing communication with sponsors, CROs, investigators, and internal site teams to support study execution.
• Support preparation for sponsor, CRO, and regulatory monitoring visits.
• Maintain inventory and organization of study equipment, supplies, and investigational products.
• Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies.
• Maintain compliance with all site SOPs, privacy standards, and research protocols.
• Perform job related duties as requested.

Skills

Blood draw

ECGs

Clinical research experience

Organizational skills

Prioritization

CTMS/EDC familiarity

Education

Associate's or Bachelor’s degree in scientific/healthcare field

Tools

CTMS or EDC systems

Job description

Iterative Health seeks a CRC I to support day‑to‑day clinical trial activities and ensure patient safety and protocol compliance. You will coordinate patient visits, collect data, and assist with regulatory requirements across GI, hepatology, obesity, and cardiology studies.

Ideal candidates have 1–3 years in clinical research or healthcare, are detail-oriented, and can manage competing priorities in a fast-paced environment while fostering strong teamwork with sponsors, CROs, and site staff.