Clinical Research Coordinator I — Drive Clinical Trials & Patient Care

TAU Ventures; Memphis (TN); On-site; USD 52,000 - 72,000; Full time

Job summary

Iterative Health is a healthcare technology and services company driving clinical research to improve patient outcomes. The CRC I will coordinate day-to-day study activities, ensure protocol compliance, and support patient safety while collaborating with sponsors, CROs, investigators, and internal teams.

The role emphasizes conducting visits, collecting data, and maintaining documentation across trials, with focus on efficiency and patient engagement in a fast-paced environment.

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline is 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, 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.
• Familiarity with CTMS or EDC systems preferred.

Responsibilities

• Support the coordination and execution of industry-sponsored clinical trials under site leadership and senior staff.
• Coordinate patient visits, procedures, and study-related activities per protocol and timelines.
• Assist with patient recruitment and retention activities including chart review and informed consent coordination.
• Conduct protocol-required patient visits and assessments per study protocols, GCP guidelines, and site SOPs.
• Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, and accountability per regulations and policy.
• Process laboratory specimens and prepare shipments per protocol and IATA regulations.
• Maintain accurate study documentation including source records, consent forms, CTMS updates, and CRFs.
• Ensure high-quality data entry and timely resolution of data queries.
• Serve as a point of contact for study participants throughout participation.
• Communicate with sponsors, CROs, investigators, and internal 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 protection of human research participants in compliance with regulations, GCP, HIPAA, and policies.
• Maintain compliance with all site SOPs, privacy standards, and protocols.
• Perform other duties as requested.

Skills

Blood draw

EKGs

Organizational skills

Prioritization

Reading protocols

CTMS/EDC familiarity

Office software

Education

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

Tools

CTMS

Job description

Iterative Health is a healthcare technology and services company driving clinical research to improve patient outcomes. The CRC I will coordinate day-to-day study activities, ensure protocol compliance, and support patient safety while collaborating with sponsors, CROs, investigators, and internal teams.

The role emphasizes conducting visits, collecting data, and maintaining documentation across trials, with focus on efficiency and patient engagement in a fast-paced environment.