Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Clinical Research Coordinator

Job

The Clinical Trials Network, LLC

Naperville, IL (In Person)

$64,151 Salary, Full-Time

Posted 2 weeks ago (Updated 1 week ago) • Actively hiring

Expires 7/1/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
80
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Clinical Research Coordinator The Clinical Trials Network, LLC Naperville, IL Job Details Full-time $25.00
  • $33.
65 an hour 1 day ago Benefits Relocation assistance Health insurance Dental insurance 401(k) Paid time off Parental leave Vision insurance 401(k) matching Life insurance Retirement plan Qualifications Computer operation Clinical research Interpersonal skills Phlebotomy Word processing Filing Productivity software Medical terminology
Full Job Description Job Summary:
The Clinical Research Coordinator's primary responsibility is to provide assistance in support of clinical research studies being conducted by the site. The Clinical Research Coordinator manages elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and company standard operating procedures. These elements include but are not limited to; day to day management of a study and study closure activities.
Responsibilities:
Leads in the recruitment of study subjects Aides in assessing eligibility of patients for participation in protocols Participates in the administration of informed consent process Responsible for the collection, entering, maintenance of data Reviews data and progress notes with CRCs and principal investigator Prepares study files for data Prepare lab kits for upcoming research visits Processes blood and urine samples for shipping Perform back-up study coordination if needed by trial schedule The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this position. It is not to be construed as an exhaustive list of duties performed by the individual so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under his/her supervision.
Other information:
  • 1 year experience in clinical research or health care field preferred
  • Understanding of medical terminology and clinical trials preferred
  • Phlebotomy experience strongly preferred
  • CMA preferred Skills required: Working knowledge of PCs and word processing and data management software Verbal and written communication Goal-oriented; self-directive Initiation, motivation, creativity Organizational and interpersonal Ability to actively participate as a team player
Job Type:
Full-time Pay:
$25.00
  • $33.
65 per hour
Benefits:
401(k) 401(k) matching Dental insurance Health insurance Life insurance Paid time off Parental leave Relocation assistance Retirement plan Vision insurance
Experience:
Phlebotomy:
1 year (Preferred) Clinical research: 1 year (Required)
Work Location:
In person