Senior Clinical Research Coordinator: Trials & Compliance

Cincinnati Children's; Cincinnati (OH); On-site; USD 52,000 - 75,000; Full time

Job summary

Cincinnati Children's is seeking a professional to support Study Conduct/Clinical Research Practice, ensuring compliance, coordinating facilities and supplies, and handling specimen collection, processing and storage per protocol.

Additionally, responsibilities include regulatory submissions, audit readiness, monitor visits, and collaboration with investigators to advance clinical studies in a compliant environment.

Qualifications

• Experience in clinical research procedures and regulatory documentation.
• Knowledge of SOPs and study conduct.

Responsibilities

• Maintain awareness of status of all active studies, arrange facilities and supplies, ensure participant and study compliance, collect, process and store specimens per protocol and SOPs, log and store specimens and maintain required records.
• Prepare, submit and maintain regulatory submissions, anticipate audits/inspections, participate in monitor visits and quality reviews, review human research protocols with authorities, determine additional requirements.

Job description

Cincinnati Children's is seeking a professional to support Study Conduct/Clinical Research Practice, ensuring compliance, coordinating facilities and supplies, and handling specimen collection, processing and storage per protocol.

Additionally, responsibilities include regulatory submissions, audit readiness, monitor visits, and collaboration with investigators to advance clinical studies in a compliant environment.