Urology Clinical Research Assistant - Data & IRB Support

Jefferson; Louisville (KY); On-site; USD 45,000 - 65,000; Full time

Job summary

Jefferson is seeking a detail-oriented research coordinator to support clinical trials by organizing and compiling data, tracking credentialing, and ensuring IRB compliance. You will collaborate with investigators and staff to maintain high-quality information and adherence to study protocols.

Under direct supervision, you will assist with IRB filings, enroll human subjects, and provide clerical and technical support to keep trial activities on schedule.

Qualifications

• High School Diploma/GED with relevant experience preferred.
• Knowledge of and ability to utilize tools, techniques and processes for gathering and reporting data in a healthcare setting.
• Knowledge of legislation and regulatory bodies affecting healthcare practices.
• Ability to manage multiple concurrent objectives, projects, groups, or activities, prioritizing effectively.

Responsibilities

• Assist research coordinators with organizing and compiling clinical research data.
• Track and maintain credentialing documentation for staff and researchers in clinical trials.
• Provide clerical and technical support to ensure adherence to study protocols and quality data.
• Inform Principal Investigator and/or designated individual of issues concerning patient response or adverse effects.
• Assist Principal Investigator with IRB filings and annual reviews.
• Assist in enrollment of human subjects.

Skills

Research data management

IRB coordination

Documentation

Clerical support

Education

High School Diploma/GED

Job description

Jefferson is seeking a detail-oriented research coordinator to support clinical trials by organizing and compiling data, tracking credentialing, and ensuring IRB compliance. You will collaborate with investigators and staff to maintain high-quality information and adherence to study protocols.

Under direct supervision, you will assist with IRB filings, enroll human subjects, and provide clerical and technical support to keep trial activities on schedule.