Senior Clinical Research Coordinator – Day Shift, Full-Time

Cincinnati Children's; Cincinnati (OH); Vor Ort; USD 57.000 - 64.000; Vollzeit

Zusammenfassung

Cincinnati Children's is seeking a detail-oriented professional to support anesthesia-related clinical research at the Burnet Campus. The role emphasizes study conduct, regulatory submissions, and participant enrollment to ensure ethical practices and compliant trials.

Responsibilities include coordinating facilities, tracking samples, and training staff while maintaining records for sponsors and regulatory authorities. A strong background in statistics and data management is preferred.

Qualifikationen

• 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.

Aufgaben

• Study Conduct/ Clinical Research Practice - Maintain awareness of status of all active studies. Arrange for facilities and supplies. Ensure participant and study compliance, i.e. collection of study specimens, and study visits. Work with study team as needed to define specimen collection, processing and storage procedures. Train others as needed to collect and label samples as instructed and deliver or process samples in accordance with the protocol, manual of operations, standard operating procedures (SOP) or other work instruction set. Ensure specimens are properly logged, handled and stored. Maintain all records and files required by regulatory agencies and sponsors. Serve as a resource for other clinical research professionals in all aspects of conducting a clinical trial. Collaborate with investigator(s) and coworkers to ensure proper progress and completion of clinical studies. Train new staff in preparation and conduct of clinical trials.

Kenntnisse

1+ years of related experience

Ausbildung

Bachelor's degree in a related field

Jobbeschreibung

Cincinnati Children's is seeking a detail-oriented professional to support anesthesia-related clinical research at the Burnet Campus. The role emphasizes study conduct, regulatory submissions, and participant enrollment to ensure ethical practices and compliant trials.

Responsibilities include coordinating facilities, tracking samples, and training staff while maintaining records for sponsors and regulatory authorities. A strong background in statistics and data management is preferred.