Clinical Research Coordinator - II

Suburban Gastroenterology Ltd

Naperville, ILFull-timePosted Apr 8, 2026

20–22 an hour

Behavioral Health Market Context

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Benefits

Dental CoveragePaid Time OffHealth Insurance

Job Description

borative work environment with room for professional growth.

Job description

The Clinical Research Coordinator's primary responsibility is to provide assistance with clinical research studies being conducted on site. The Clinical Research Coordinator II helps manage 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 assisting with the day-to-day management of a study and study closure activities.

Responsibilities:
• Helps in the recruitment of study subjects
• Aides in assessing eligibility of patients for participation in protocols
• Participates in the administration of informed consent process
• Assists with the collection, entering, maintenance of data
• Reviews data and progress notes with CRCs and principal investigator
• Prepares study files for data
• Prepares 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

Experience:
• Phlebotomy: 1 year (Preferred)
• Clinical research: 1 year (Required)

Work Location: In person

Join our team as a Clinical Research Coordinator and contribute to our mission of delivering exceptional healthcare services. If you are passionate about making a difference in the healthcare industry and possess the required skills, we invite you to apply today to be part of our dedicated team. Please email cover letter and resume to [email protected]

Job Type: Full-time

Pay: $20.00 - $22.00 per hour

Benefits:
• 401(k)
• Dental insurance
• Employee assistance program
• Employee discount
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance

Medical Specialty:
• Gastroenterology

Work Location: In person

Qualifications

  • 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
  • Clinical research: 1 year (Required)
  • Gastroenterology

Benefits

  • Pay: $20.00 - $22.00 per hour
  • 401(k)
  • Dental insurance
  • Employee assistance program
  • Employee discount
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Vision insurance

Responsibilities

  • The Clinical Research Coordinator's primary responsibility is to provide assistance with clinical research studies being conducted on site
  • The Clinical Research Coordinator II helps manage 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 assisting with the day-to-day management of a study and study closure activities
  • Helps in the recruitment of study subjects
  • Aides in assessing eligibility of patients for participation in protocols
  • Participates in the administration of informed consent process
  • Assists with the collection, entering, maintenance of data
  • Reviews data and progress notes with CRCs and principal investigator
  • Prepares study files for data
  • Prepares 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


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