Clinical Research Coordinator I — Autism & Neurodevelopment

Nationwide Children's Hospital Inc

Columbus (OH)

On-site

USD 52,000 - 66,000

Full time

4 days ago
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Job summary

Nationwide Children's Hospital Inc. is seeking a Clinical Research Coordinator I to manage elements of pediatric clinical studies in compliance with ICH/GCP and institutional SOPs.

The role includes start-up, conduct, and close-out activities, with emphasis on data integrity and patient safety. You will recruit and enroll participants, oversee data collection and specimen processing, coordinate visits, and ensure regulatory documentation is complete.

Qualifications

  • Understanding of medical terminology and clinical research preferred.
  • Excellent communication skills in verbal and written form.
  • Strong organizational and interpersonal abilities.

Responsibilities

  • Recruits, consents and enrolls subjects according to ICH/GCP and IRB requirements; acts as patient/family advocate.
  • Ensures eligibility criteria are met and flags safety concerns or protocol deviations.
  • Collects and manages study data; maintains accurate data collection and laboratory procedures.
  • Prepares and processes human specimens; may perform CLIA waived tests.
  • Schedules subject visits with PI/sub-I and other services; maintains regulatory binder.
  • Completes Case Report Forms accurately and on time.
  • Participates as a team member; adheres to SOPs and quality control guidelines.

Skills

Medical terminology
Clinical research understanding
Analytical skills
Verbal and written communication
Organizational skills
Team player

Education

Associates degree, STNA, PCA, LPN, MA or equivalent
BA/BS preferred

Job description

Nationwide Children's Hospital Inc. is seeking a Clinical Research Coordinator I to manage elements of pediatric clinical studies in compliance with ICH/GCP and institutional SOPs.

The role includes start-up, conduct, and close-out activities, with emphasis on data integrity and patient safety. You will recruit and enroll participants, oversee data collection and specimen processing, coordinate visits, and ensure regulatory documentation is complete.

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