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Clinical Research Coordinator II

Iterative Health
Location
Rochester, New York
Posted
26 days ago
Department
MSO
What they actually want (must-haves)
  • Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required
  • 3-5 years of clinical research or healthcare experience required
  • 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 preferred
  • CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification preferred
  • Familiarity with CTMS or EDC systems preferred
What the job really is

As a Clinical Research Coordinator II at Iterative Health, you will independently manage and coordinate daily activities of clinical trials, ensuring compliance with protocols and regulatory standards. Your role will involve patient recruitment, conducting assessments, managing study documentation, and serving as a primary contact for study participants. You will also support process improvements and maintain communication with various stakeholders to ensure successful study execution.

Things to weigh
  • No specific mention of remote work options or flexible hours
  • Pay range provided, but no specific salary details for the role
  • Requires managing complex studies with minimal oversight, which may indicate a high level of responsibility
  • Physical requirements include the ability to lift and move up to 25 pounds, which may be a consideration for some candidates
Job score2.8/5
Benefits1/5
Freshness4/5
Career value4/5
Role clarity5/5
Pay transparency0/5

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