Senior Clinical Research Coordinator

Cincinnati Children's; Cincinnati (OH); On-site; USD 57,000 - 64,000; Full time

Job summary

Cincinnati Children’s is seeking a day-shift, full-time professional in Psychiatry at the Burnet Campus to support clinical research operations. You will conduct studies, coordinate regulatory submissions, recruit participants, maintain communications with sponsors and teams, and manage data for multiple studies.

Required is a Bachelor’s degree in a related field and 1+ years of experience (or a Master’s degree).

Qualifications

• Bachelor's degree in a related field.
• 1+ years of directly related experience OR Master's degree in a related field.
• Knowledge of statistical process control principles.

Responsibilities

• Study Conduct/ Clinical Research Practice - maintain awareness of status of all active studies and ensure participant and study compliance.
• Regulatory Compliance and Documentation - prepare and maintain regulatory submissions accurately and timely.
• Recruitment/Enrollment/Retention - identify potential participants and maintain tracking for enrollment and retention.
• Communication - compose and maintain all study correspondence and liaise with internal and external teams.
• Data Management - create CRFs, ensure accuracy, and support data-management processes.

Skills

Statistical process control

Education

Bachelor's degree in a related field

1+ years of directly related experience OR Master's degree in a related field

Job description

Cincinnati Children’s is seeking a day-shift, full-time professional in Psychiatry at the Burnet Campus to support clinical research operations. You will conduct studies, coordinate regulatory submissions, recruit participants, maintain communications with sponsors and teams, and manage data for multiple studies.

Required is a Bachelor’s degree in a related field and 1+ years of experience (or a Master’s degree).