Senior Clinical Research Coordinator, Pediatrics

CO00 Children's Hospital Medical Center

Greendale (WI)

On-site

USD 57,000 - 62,000

Full time

14 days+

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Job summary

Cincinnati Children's Hospital Medical Center is seeking talented Clinical Research Coordinators (CRCs) to support innovative clinical and translational research programs across a wide range of specialties.

CRCs may coordinate participant recruitment and enrollment, conduct study visits, manage regulatory documentation, collect and process research specimens, oversee study data, collaborate with multidisciplinary teams, and ensure compliance with research protocols and regulatory requirements.

Qualifications

  • Bachelor's degree in a scientific, healthcare, public health, psychology, or related field and at least one year of related work experience OR a Master's degree.
  • Strong organizational, communication, and problem-solving skills.
  • Proficiency with Microsoft Office applications.

Responsibilities

  • Coordinating day-to-day research study activities.
  • Recruiting, screening, consenting, and retaining study participants.
  • Scheduling and conducting study visits.
  • Maintaining research records and source documentation.
  • Managing regulatory submissions and study approvals.
  • Entering and validating study data in electronic databases.
  • Collaborating with investigators, sponsors, clinical teams, and research participants.
  • Supporting study monitoring visits, audits, and quality assurance activities.

Skills

Study coordination
Regulatory compliance
Communication skills

Education

Bachelor's degree in scientific/healthcare/public health/psychology or related field
Master's degree

Tools

REDCap
Medidata
OnCore

Job description

Cincinnati Children's Hospital Medical Center is seeking talented Clinical Research Coordinators (CRCs) to support innovative clinical and translational research programs across a wide range of specialties.

CRCs may coordinate participant recruitment and enrollment, conduct study visits, manage regulatory documentation, collect and process research specimens, oversee study data, collaborate with multidisciplinary teams, and ensure compliance with research protocols and regulatory requirements.

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