Clinical Research Coordinator I - Impactful Trials

TAU Ventures; Webster (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

Iterative Health is a healthcare technology and services company accelerating clinical research to improve patient outcomes. The CRC I will help execute industry-sponsored trials, coordinate patient visits, ensure protocol adherence, and maintain compliance with GCP, HIPAA, and site SOPs.

You will work with patients, sponsors, CROs, investigators, and internal teams to deliver high-quality clinical research and support data integrity and patient safety throughout the study lifecycle.

Qualifications

• Requires an Associate’s or Bachelor's degree in a scientific, healthcare, or related discipline.
• 1–3 years of clinical research or healthcare experience required.
• Ability to perform blood draws, vital signs, and EKGs per state law where applicable.

Responsibilities

• Coordinate patient visits, procedures, and study-related activities per protocol and timelines.
• Support patient recruitment, chart reviews, scheduling, and informed consent coordination.
• Maintain study documentation, data entry, and query resolution with accuracy and timeliness.
• Serve as a point of contact for study participants and communicate with sponsors, CROs, and internal teams.
• Assist preparation for regulatory monitoring visits and ensure compliance with HIPAA and GCP.

Skills

Blood draw

EKGs

Clinical research

CTMS / EDC

Office software

Attention to detail

Education

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

Tools

CTMS / EDC

Microsoft Office

Job description

Iterative Health is a healthcare technology and services company accelerating clinical research to improve patient outcomes. The CRC I will help execute industry-sponsored trials, coordinate patient visits, ensure protocol adherence, and maintain compliance with GCP, HIPAA, and site SOPs.

You will work with patients, sponsors, CROs, investigators, and internal teams to deliver high-quality clinical research and support data integrity and patient safety throughout the study lifecycle.