Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Apply Offsite

Norton Healthcare

Clinical Research Assistant, Norton Cancer Institute Research Operations St. Matthews Days

Pay: Not specified

Posted: 3 weeks ago

Location: Louisville, KY (Onsite)

Last Updated: 1 week ago

Hours: Full-Time

Expires: 10/6/2026

Career Insights for Clinical Research Associate

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on Kentucky data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Clinical Research Associate is responsible for running clinical trials, usually for an organization undertaking pharmacological drug testing. Will ensure that trials adhere to good clinical practice guidelines for monitoring clinical trials.

$106,151 / year median in Kentucky

+2% projected growth

Explore Career

Job Description

Clinical Research Assistant, Norton Cancer Institute Research Operations St. Matthews Days Norton Healthcare - 3.8 Louisville, KY Job Details Full-time 4 hours ago Qualifications Laboratory inventory control CCRC Laboratory equipment maintenance Medical equipment operation CCRA Research project coordination Data reporting support Medical record abstraction Research compliance clinical trial records management Order placement Implementing research protocols CCRP Research participation Associate's degree Entry level Quality data entry

Full Job Description Responsibilities:

Clinical Research Assistant (CRA) provides support to the research team by collecting, entering, abstracting, and managing the study data for sponsor data systems, publication, or other reporting. The CRA may also assist the Clinical Research Nurse (CRN) and/or Clinical Research Coordinator (CRC) in the set-up and execution of clinical research protocol procedures and associated administrative responsibilities. In some cases, the CRA may coordinate retrospective, quality, and other non-therapeutic research trials under Principal Investigator direction. Additionally, the CRA is responsible to maintain research medical equipment; accurately maintain logs; perform protocol-related tasks as assigned (within scope of practice); inventory, store, order and maintain study-related equipment/ supplies.

Qualifications:

Required:

One year in a research or healthcare setting

Desired:

One year in data entry or abstraction Associate Degree Certified Clinical Data Manager OR Certified Clinical Research Associate OR Certified Clinical Research Coordinator OR Certified Clinical Research Professional OR Certified Medical Assistant OR Certified Tumor Registrar