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Clinical Research Coordinator II

Iterative Health
Location
Waterford, Connecticut
Posted
27 days 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® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional 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 independently manage and coordinate clinical trials, ensuring compliance with protocols and regulatory standards. Your responsibilities include overseeing patient recruitment, conducting required assessments, maintaining study documentation, and serving as a primary contact for study participants. You will also collaborate with various stakeholders to resolve study-related issues and support process improvements.

Things to weigh
  • No salary information provided
  • Role requires managing complex studies with minimal oversight, which may be challenging for less experienced candidates
  • 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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