Urology Clinical Research Coordinator

First Urology; Jeffersonville, Northern (IN, KY); Hybrid; USD 52,000 - 70,000; Full time

Benefits offered by this job

401(k) match

Health insurance

Vision insurance

Life insurance

AD&D

Long-term disability

Sick days

Holidays

Vacation time

Milestone checks

Vacation cabin

Job summary

First Urology is seeking a Research Clinical Coordinator to oversee clinical trials within our urology practice. You will coordinate all aspects of trials, ensure compliance with study protocols, and deliver an exceptional patient experience.

The ideal candidate has 2+ years of clinical research experience and strong knowledge of FDA regulations, GCP, and human subject protections, with solid organizational and communication skills. This is a full-time, in-office role supporting multiple studies.

Qualifications

• 2+ years of clinical research experience preferred.
• Knowledge of FDA regulations, GCP, and human subject protection standards.
• Strong organizational, documentation, and time management skills.
• Excellent communication and interpersonal skills.

Responsibilities

• Oversee the smooth operation of clinical trials.
• Collect, code and analyze data from research activities.
• Communicate study objectives with participants.
• Administer questionnaires and monitor participant adherence to study rules.
• Liaise with laboratories regarding research findings.
• Ensure protocol compliance and regulatory standards.
• Maintain study records including case report forms and drug dispensation.
• Direct collection, labeling, storage and transport of specimens.
• Ensure equipment and supplies for the study are in stock and functional.

Skills

General Office/Clinical task

Communication

Organization

Time management

Education

High school diploma or equivalent

Associate degree or higher

Job description

First Urology is seeking a Research Clinical Coordinator to oversee clinical trials within our urology practice. You will coordinate all aspects of trials, ensure compliance with study protocols, and deliver an exceptional patient experience.

The ideal candidate has 2+ years of clinical research experience and strong knowledge of FDA regulations, GCP, and human subject protections, with solid organizational and communication skills. This is a full-time, in-office role supporting multiple studies.