Clinical Research Coordinator II/III — Endocrinology Trials

CO00 Children's Hospital Medical Center; United States; On-site; USD 51,000 - 64,000; Full time

Job summary

Cincinnati Children's seeks a Clinical Research Coordinator II/III to support endocrine studies and regulatory submissions. You will oversee study conduct, participant recruitment, data management, and team training in a collaborative environment.

The role emphasizes compliance, documentation, and communication with sponsors and investigators to ensure timely study progress and high-quality data.

Qualifications

• High school diploma or equivalent and 2 years of related work experience.
• Preferred: Bachelor's degree in a related field.
• CRC II/CRC III roles require relevant education and study experience.

Responsibilities

• Study conduct/clinical research: manage active studies, ensure compliance and proper specimen handling.
• Regulatory compliance and documentation: prepare submissions and maintain accurate records.
• Recruitment/enrollment/retention: identify and screen participants and track progression.
• Communication: liaise with departments, sponsors, and investigators to resolve issues.
• Data management: create CRFs, enter data, and perform data quality checks.

Skills

Regulatory compliance

Documentation

Recruitment

Data management

Communication

Clinical research

Education

High school diploma or equivalent

Bachelor's degree in a related field

Bachelor's degree in a related field

Master's degree in a related field

Job description

Cincinnati Children's seeks a Clinical Research Coordinator II/III to support endocrine studies and regulatory submissions. You will oversee study conduct, participant recruitment, data management, and team training in a collaborative environment.

The role emphasizes compliance, documentation, and communication with sponsors and investigators to ensure timely study progress and high-quality data.