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Clinical Research Coordinator II - Beaumont, TX

Iterative Health
Location
Beaumont, Texas
Posted
1 month ago
Department
MSO
What they actually want (must-haves)
  • Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline
  • 3-5 years of clinical research or healthcare experience
  • Strong organizational skills and attention to detail
  • Ability to manage competing priorities in a fast-paced environment
  • Ability to read, interpret, and apply research protocols and clinic policies
  • Proficiency with CTMS, EDC systems, and standard office software applications
Nice to have
  • Experience in gastroenterology, hepatology, cardiology therapeutic areas
  • CCRC® or CCRP® certification or equivalent clinical research certification
  • Familiarity with CTMS or EDC systems
What the job really is

As a Clinical Research Coordinator II at Iterative Health, you will manage and coordinate clinical trials, ensuring compliance with protocols and regulatory standards. Your responsibilities include patient recruitment, conducting assessments, maintaining study documentation, and serving as a primary contact for study participants. You will work closely with various stakeholders to drive study execution and address any issues that arise during the trial process.

Things to weigh
  • No salary listed
  • Role requires managing complex studies with minimal oversight
  • Physical requirements include the ability to lift and move up to 25 pounds
Job score2.8/5
Benefits1/5
Freshness4/5
Career value4/5
Role clarity5/5
Pay transparency0/5

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