Clinical Research Coordinator I: Join Fast-Moving Trials

iterativehealth

City of Albany (NY)

On-site

USD 55,000 - 75,000

Full time

7 days ago
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Job summary

Iterative Health is seeking a Clinical Research Coordinator I in Albany, NY to support industry-sponsored trials and patient care. You will coordinate patient visits, consent processes, and data collection while ensuring protocol compliance and patient safety.

You will work with sponsors, CROs, investigators, and internal teams to keep studies on track. The role requires 1–3 years of clinical research or healthcare experience, a scientific/healthcare degree, and ability to perform select

Qualifications

  • Bachelor's or associate degree in a scientific/healthcare field is required.
  • 1-3 years of clinical research or healthcare experience are required.
  • Ability to perform blood draws and ECGs where state law allows.
  • Proficiency with standard office software and willingness to learn trial systems.

Responsibilities

  • Coordinate patient visits, procedures, and study activities per protocol.
  • Support patient recruitment, outreach, scheduling, and consent coordination.
  • Conduct protocol visits and assessments in line with GCP and SOPs.
  • Perform clinical procedures including vital signs and specimen collection as allowed.
  • Ensure accurate documentation, CTMS/EDC updates, and data queries resolution.
  • Maintain inventory and assist with study shipments and regulatory readiness.
  • Communicate with sponsors, CROs, investigators, and site teams regularly.

Skills

Organization
Attention to detail
Prioritization
Communication

Education

Associate's or Bachelor's degree in a scientific/healthcare field

Tools

CTMS
EDC systems
Office software

Job description

Iterative Health is seeking a Clinical Research Coordinator I in Albany, NY to support industry-sponsored trials and patient care. You will coordinate patient visits, consent processes, and data collection while ensuring protocol compliance and patient safety.

You will work with sponsors, CROs, investigators, and internal teams to keep studies on track. The role requires 1–3 years of clinical research or healthcare experience, a scientific/healthcare degree, and ability to perform select

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