Clinical Research Coordinator - Flowood, MS

Iterative Health•Flowood, MS

11h•Onsite

About The Position

Iterative Health is a healthcare technology and services company focused on accelerating clinical research to improve patient outcomes. The Iterative Health Site Network includes over 70 clinical research sites in the US and Europe, specializing in gastrointestinal (GI) and hepatology therapies. The company aims to support the success and growth of its partner sites through tech-enabled services, combining clinical trial expertise with AI to help research teams and sponsors expedite access to novel therapeutics. This is a full-time position for an experienced Clinical Research Coordinator (CRC) who will support, facilitate, and coordinate daily clinical trial activities, playing a crucial role in study execution.

Requirements

Minimum 1-2 years of clinical research experience.
Able to execute research tasks with guidance from more experienced staff, PIs, and management.
Strong written and verbal communication skills.
Ability to read, interpret, and apply clinic policies and research protocols.
Ability to use standard office software.
Must be able to lift up to 25 pounds.

Nice To Haves

Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred.

Responsibilities

Administratively and clinically manage industry-sponsored clinical trials, including problem-solving, communication, and protocol management.
Lead patient recruitment activities, such as performing chart reviews, discussing protocols with patients, and verifying informed consent documentation.
Schedule all patient research visits and procedures according to protocol requirements.
Conduct patient visits as outlined in each study protocol.
Dispense study medication, collect vital signs, and perform ECGs.
Perform blood draws, and process and ship specimens according to study protocol and IATA regulations.
Ensure relevant study and subject-specific information is entered into the CTMS system regularly.
Complete and maintain study files, including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms.
Act as the point of contact for study participants.
Adhere to Research SOPs, Good Clinical Practices, and study protocols.
Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, and PI throughout the study.
Ensure all safety data is reviewed by the PI in a timely manner.
Maintain an inventory of study equipment and supplies onsite.
Participate actively in communicating status and results to management.
Assist with routine data verification and quality control to ensure data integrity and consistency with the study protocol.
Schedule and prepare for monitor visits.
Assist the Study Team in protecting the rights and welfare of human research participants in accordance with Federal regulations.
Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and report 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.