Clinical Research Coordinator I — Patient‑Centric Trials

Socket.dev; Memphis (TN); On-site; USD 52,000 - 70,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator I to support the execution of industry-sponsored clinical trials and enhance the patient research experience. You will coordinate patient visits, procedures, and study activities while ensuring protocol compliance, regulatory standards, and participant safety.

The role involves collaboration with patients, sponsors, CROs, investigators, and internal teams to deliver high-quality research and contribute to innovative therapies.

Qualifications

• Bachelor’s or associate’s degree in a scientific, healthcare, or related discipline.
• 1–3 years of clinical research or healthcare experience.
• Blood draw, blood pressure, height, weight measurements, and ECGs as allowed by state law.
• Proficiency with standard office software; 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.
• Process laboratory specimens and prepare shipments in accordance with 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 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

Organizational skills

Attention to detail

Prioritization

Office software proficiency

Communication with stakeholders

CTMS/EDC familiarity

Education

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

Tools

CTMS/EDC systems

Job description

Iterative Health is seeking a Clinical Research Coordinator I to support the execution of industry-sponsored clinical trials and enhance the patient research experience. You will coordinate patient visits, procedures, and study activities while ensuring protocol compliance, regulatory standards, and participant safety.

The role involves collaboration with patients, sponsors, CROs, investigators, and internal teams to deliver high-quality research and contribute to innovative therapies.