Onsite Clinical Research Coordinator II — Study Ops

University of Kentucky; Lexington (KY); Hybrid; USD 45,000 - 60,000; Full time

Job summary

The University of Kentucky is seeking a Clinical Research Coordinator II for the Markey Cancer Center Clinical Research Organization. The primary duties include data collection, reporting, and coordinating workflow for clinical studies, while ensuring adherence to GCP/SOP and protocol requirements.

This onsite role involves patient flow management, collaboration with health professionals, and ongoing documentation.

Qualifications

• Strong attention to detail and excellent organizational skills.
• Proficient in operating office machines including computers and printers.
• Robust interpersonal skills and strong written/verbal communication.
• Advanced knowledge of Microsoft Office products.
• Ability to take initiative and manage time effectively.

Responsibilities

• Obtain, abstract and collate data, reports and forms for studies.
• Maintain and submit reports and updated records as required by the study.
• Assist in designing systems to organize and plan workflow for clinical studies.
• Coordinate patient flow through clinical studies and monitor events.
• Ensure protocol compliance and communicate with PI and health professionals.

Skills

Attention to detail

Organizational skills

Office software

Interpersonal skills

Microsoft Office

Written & verbal communication

Initiative

Time management

Technical skills

Collaboration

Tools

Computers

Printers

Job description

The University of Kentucky is seeking a Clinical Research Coordinator II for the Markey Cancer Center Clinical Research Organization. The primary duties include data collection, reporting, and coordinating workflow for clinical studies, while ensuring adherence to GCP/SOP and protocol requirements.

This onsite role involves patient flow management, collaboration with health professionals, and ongoing documentation.