Clinical Research Coordinator I: Fast-Track Trials & Impact

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

Job summary

Iterative Health in the United States is hiring a Clinical Research Coordinator to support daily clinical trial activities across sites. The role focuses on patient recruitment, consent discussions, visit scheduling, data entry, and adherence to GCP and protocol requirements.

Responsibilities include administering study procedures, collecting vital signs, coordinating with PI, CROs, and sponsors, handling study medication, and maintaining study files.

Qualifications

• Minimum 1–2 years of clinical research experience.
• Strong written and verbal communication skills.
• Ability to read, interpret, and apply clinic policies and research protocols.
• Ability to use standard office software.

Responsibilities

• Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management.
• Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation
• Schedule all patient research visits and procedures consistent with protocol requirements
• Conduct patient visits as outlined within each study protocol
• Dispense study medication, collect vital signs and perform ECGs
• Perform blood draws, process and ship specimens per study protocol and IATA regulations
• Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation
• Act as point of contact for study participants
• Adhere to Research SOPs, Good Clinical Practices, and the study protocols
• Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout course of the study
• Ensure all safety data is reviewed by the PI in a timely manner
• Maintain inventory of study equipment and supplies onsite at all times
• Participate actively in communication of status and results to management
• Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol
• Schedule and prepare for monitor visits
• Assists Study Team in protection of the rights and welfare of all human research participants
• Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance
• Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy

Skills

Communication skills

Education

Clinical or scientific discipline degree (Associate/Bachelor) preferred

Job description

Iterative Health in the United States is hiring a Clinical Research Coordinator to support daily clinical trial activities across sites. The role focuses on patient recruitment, consent discussions, visit scheduling, data entry, and adherence to GCP and protocol requirements.

Responsibilities include administering study procedures, collecting vital signs, coordinating with PI, CROs, and sponsors, handling study medication, and maintaining study files.