Clinical Research Coordinator I - Port Arthur, TX

Minimum 1-2 years of clinical research experience

Ability to read, interpret, and apply clinic policies and research protocols

At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves.

At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves.

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