Senior CRC: Complex Multicenter Clinical Trials

Cincinnati Children's

Cincinnati (OH)

Presencial

USD 57.000 - 81.000

Jornada completa

hace 34 horas
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Descripción de la vacante

Cincinnati Children’s Hospital Medical Center is seeking a seasoned Clinical Research Coordinator in Pulmonary Medicine to lead complex, multi-center trials. You will supervise staff, oversee regulatory processes, and guide recruitment from start to finish while ensuring data quality and protocol compliance.

The role emphasizes collaboration with investigators, cross-divisional teams, and adherence to SOPs, with a focus on patient safety and study integrity in a high-volume clinical setting.

Formación

  • Bachelor's degree in a related field required. Master’s preferred for CRC IV.
  • CCR III/IV certification enhances eligibility and progression.
  • Clinical research coordination knowledge and SOP adherence essential.

Responsabilidades

  • Study Conduct/Clinical Research Practice: serve as a resource for all aspects of conducting a complex, multi-center trial and guide staff under PI supervision.
  • Regulatory Compliance and Documentation: coordinate regulatory activities, maintain records, and ensure timely submissions and audits.
  • Recruitment/Enrollment/Retention: oversee staff, identify and enroll participants, and monitor recruitment progress against timelines.
  • Data Management: oversee data entry/validation, create CRFs/data dictionaries, and ensure data quality and integrity.

Educación

Bachelor's degree in a related field
Master's degree in a related field
Certified Clinical Research Coordinator

Descripción del empleo

Cincinnati Children’s Hospital Medical Center is seeking a seasoned Clinical Research Coordinator in Pulmonary Medicine to lead complex, multi-center trials. You will supervise staff, oversee regulatory processes, and guide recruitment from start to finish while ensuring data quality and protocol compliance.

The role emphasizes collaboration with investigators, cross-divisional teams, and adherence to SOPs, with a focus on patient safety and study integrity in a high-volume clinical setting.

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