Iterative Health · 1 month ago
Clinical Research Coordinator
Tupelo, MS
Full-time
Hybrid
Entry Level
1+ years expIterative Health is a healthcare technology and services company focused on transforming patient outcomes through clinical research. They are seeking a full-time Clinical Research Coordinator to manage daily clinical trial activities, facilitate patient recruitment, and ensure compliance with study protocols.
Health CareInformation Technology
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
Qualification
Required
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
Must be able to lift up to 25 pounds
Preferred
Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related discipline preferred
Company
Iterative Health
Iterative Health develops technology that can benefit patients anywhere, regardless of socioeconomic or geographic barriers.
51-200 employees
Funding
Current Stage
Growth StageTotal Funding
unknown2019-01-01Seed
Leadership Team
Jonathan Ng
CEO
Bill Kayser
President & CFO
Recent News
2025-10-01
2025-09-30
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