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Clinical Research Coordinator

Iterative Health

Salary not specified
Dec 16, 2025
Flowood, MS, US
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Iterative Health aims to accelerate clinical research and transform patient outcomes by empowering clinical research sites with tech-enabled services, particularly in gastrointestinal (GI) and hepatology novel therapies.

Requirements

  • Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred
  • Minimum 1-2 years of clinical research experience
  • 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 study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.

Other

  • Strong written and verbal communication skills
  • Must be able to lift up to 25 pounds