Senior Clinical Research Coordinator — Allergy & Immunology

Cincinnati Children's Hospital Medical Center

United States

On-site

USD 57,000 - 80,000

Full time

4 days ago
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Job summary

Cincinnati Children’s Hospital Medical Center is seeking an experienced Clinical Research Coordinator (CRC) to join the Risma Lab in the Division of Allergy and Immunology.

The role involves coordinating clinical and translational research on adverse drug reactions, with responsibilities across study conduct, regulatory compliance, recruitment, data management, and communication with sponsors and clinical teams.

Qualifications

  • Required for CRC III: Bachelor's degree in a related field, and 1 year of directly related work experience, or a Master's degree in a related field.
  • Required for CRC IV: Bachelor's degree in a related field with 3 years of experience in related job discipline or Master's degree and 2 years of experience in a related job discipline.
  • Certified Clinical Research Coordinator within 18 months of external hire date.

Responsibilities

  • Study Conduct/Clinical Research Practice: maintain awareness of status of all active studies and ensure participant and study compliance.
  • Regulatory Compliance and Documentation: manage regulatory submissions, audits, and approvals and maintain study records.
  • Recruitment/Enrollment/Retention: identify eligible participants, conduct pre-consent screening, and execute informed consent.
  • Data Management: create CRFs, enter data, and perform data cleaning and quality checks.
  • Communication: liaise with internal departments, sponsors, and study teams to ensure smooth study conduct.

Education

Bachelor's degree in a related field
Master's degree in a related field

Job description

Cincinnati Children’s Hospital Medical Center is seeking an experienced Clinical Research Coordinator (CRC) to join the Risma Lab in the Division of Allergy and Immunology.

The role involves coordinating clinical and translational research on adverse drug reactions, with responsibilities across study conduct, regulatory compliance, recruitment, data management, and communication with sponsors and clinical teams.

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