Clinical Research Coordinator I — Patient-Focused Trials

Iterative-Health; Webster (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

Iterative Health, a healthcare technology and services company, seeks a Clinical Research Coordinator I in Webster, TX to support day-to-day study activities and ensure protocol compliance. You will work with patients, sponsors, CROs, investigators, and internal teams to deliver high-quality clinical research and advance innovative therapies.

Responsibilities include coordinating visits, exams, data entry, and specimen handling, while maintaining source documentation and regulatory readiness.

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, 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 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

Blood draw

EKG

Clinical research

Data entry

Regulatory knowledge

CTMS/EDC familiarity

Education

Bachelor’s degree in science/healthcare

Tools

CTMS

EDC systems

MS Office

Job description

Iterative Health, a healthcare technology and services company, seeks a Clinical Research Coordinator I in Webster, TX to support day-to-day study activities and ensure protocol compliance. You will work with patients, sponsors, CROs, investigators, and internal teams to deliver high-quality clinical research and advance innovative therapies.

Responsibilities include coordinating visits, exams, data entry, and specimen handling, while maintaining source documentation and regulatory readiness.