Clinical Research Coordinator I - Memphis, TN

Iterative Health•Memphis, TN

18d

About The Position

The Clinical Research Coordinator I supports the successful execution of clinical trials and the patient research experience. The role coordinates day-to-day study activities under the guidance of site leadership and senior research staff, ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines. The coordinator works with patients, sponsors, CROs, investigators, and internal teams to deliver high-quality clinical research and contribute to the advancement of innovative therapies.

Requirements

Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline.
1–3 years of clinical research or healthcare experience.
Ability to perform blood draws, medical reviews (including blood pressure, height, and weight), and EKGs, as applicable by state law.
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.
Ability to sit, stand, and move throughout clinical and office environments for extended periods.
Ability to lift and move up to 25 pounds as needed.

Nice To Haves

Familiarity with CTMS or EDC systems.

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 activities in accordance with protocol requirements and study timelines.
Support patient recruitment and retention through chart review, 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 regulations, training, and organizational policy.
Process laboratory specimens and prepare shipments according to protocol requirements and applicable IATA regulations.
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 their study participation.
Communicate with sponsors, CROs, investigators, and internal site teams to support study execution.
Support preparation for sponsor, CRO, and regulatory monitoring visits.
Maintain the inventory and organization of study equipment, supplies, and investigational products.
Protect human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies.
Maintain compliance with site SOPs, privacy standards, and research protocols.
Perform other job-related duties as requested.