Clinical Research Coordinator I - Patient-Focused Trials

TAU Ventures; Port Arthur (TX); On-site; USD 52,000 - 78,000; Full time

Job summary

Iterative Health is seeking a full-time, experienced Clinical Research Coordinator (CRC) to support daily trial activities and coordinate studies. The role includes managing patient visits, data collection, CTMS entry, consent, and samples, while ensuring protocol, SOP, and GCP compliance.

Ideal candidates have 1–2 years of clinical research experience and a clinical/science degree. On-site role with collaboration across sites and with CROs and PIs.

Qualifications

• Minimum 1-2 years of clinical research experience.
• Bachelor’s degree or higher in a clinical or scientific discipline preferred.
• Strong written and verbal communication skills.

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 study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.
• 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 involved in research in accordance with Federal regulations
• 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

Clinical research

Communication skills

Medical terminology

Education

Bachelor’s degree or higher in clinical or scientific-related discipline

1-2 years of clinical research experience

Job description

Iterative Health is seeking a full-time, experienced Clinical Research Coordinator (CRC) to support daily trial activities and coordinate studies. The role includes managing patient visits, data collection, CTMS entry, consent, and samples, while ensuring protocol, SOP, and GCP compliance.

Ideal candidates have 1–2 years of clinical research experience and a clinical/science degree. On-site role with collaboration across sites and with CROs and PIs.