Senior Clinical Research Coordinator

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

Zusammenfassung

Cincinnati Children’s, Burnet Campus, is seeking a Clinical Research professional to join the Clinical Research Services team. The role is full-time, day shift, 40 hours per week, with ongoing opportunities to contribute to compliant and high-quality studies.

Starting pay ranges reflect experience and equity considerations. The position emphasizes study conduct, regulatory documentation, recruitment, and data management, requiring collaboration with investigators, sponsors, and clinical teams to

Qualifikationen

• Bachelor's degree in a related field.
• 1+ years of directly related experience or a 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 and coordinate facilities, supplies, and visits.
• Regulatory Compliance and Documentation: submit regulatory documents, audits, and ensure regulatory readiness.
• Recruitment/Enrollment/Retention: identify eligible participants, track progress, and manage consent and enrollment.
• Communication: maintain correspondence and serve as liaison to internal and external partners.
• Data Management: create CRFs, ensure data accuracy, and enter data into databases.
• Train staff to collect, label and process samples per SOPs; ensure proper handling and storage.

Kenntnisse

Statistical process control

Ausbildung

Bachelor's degree in related field

Master's degree in related field

Jobbeschreibung

Cincinnati Children’s, Burnet Campus, is seeking a Clinical Research professional to join the Clinical Research Services team. The role is full-time, day shift, 40 hours per week, with ongoing opportunities to contribute to compliant and high-quality studies.

Starting pay ranges reflect experience and equity considerations. The position emphasizes study conduct, regulatory documentation, recruitment, and data management, requiring collaboration with investigators, sponsors, and clinical teams to