Clinical Research Associate (CRA) I
- Spectraforce Technologies
- North Chicago, Illinois
- Full Time
Clinical Research Associate (CRA) I
Spectraforce Technologies
United States, Illinois, North Chicago
Mar 18, 2026
Position Title: Clinical Research Associate
Work Location: North Chicago, IL
Assignment Duration: 12 Months (With Potential Extension)
Work Schedule: 40 hours day shift.
Work Arrangement: Onsite
Position Summary: Review protocols and comply with study-specific activities. Communicates in an appropriate and professional manner with study subjects and unit personnel.
Background & Context: This role is within the Clinical Pharmacology & Pharmacometrics Research Unit of our organization.
Key Responsibilities:
Review protocols and comply with study-specific activities
Communicates in an appropriate and professional manner with study subjects and unit personnel.
Maintain accurate and complete source data.
Perform study protocol related activities, i.e. phlebotomy, sample processing, ECG collection, vital signs, height/weight, etc., as assigned.
Maintain safety and confidentiality of study subjects throughout the study.
Understands and complies with SOPs, FDA regulations, and basic GCP requirements.
Qualification & Experience:
Minimum Education Required: High School Diploma or equivalent
Preferred Education: Clinical Medical Assistant, EMT, Paramedic, military medic with recent clinical experience, or higher
1-2 years of work experience in a clinical or research environment, or in a patient care setting; and
1-2 years of work experience in a role with phlebotomy responsibilities
Spectraforce Technologies
United States, Illinois, North Chicago
Mar 18, 2026
Position Title: Clinical Research Associate
Work Location: North Chicago, IL
Assignment Duration: 12 Months (With Potential Extension)
Work Schedule: 40 hours day shift.
Work Arrangement: Onsite
Position Summary: Review protocols and comply with study-specific activities. Communicates in an appropriate and professional manner with study subjects and unit personnel.
Background & Context: This role is within the Clinical Pharmacology & Pharmacometrics Research Unit of our organization.
Key Responsibilities:
Review protocols and comply with study-specific activities
Communicates in an appropriate and professional manner with study subjects and unit personnel.
Maintain accurate and complete source data.
Perform study protocol related activities, i.e. phlebotomy, sample processing, ECG collection, vital signs, height/weight, etc., as assigned.
Maintain safety and confidentiality of study subjects throughout the study.
Understands and complies with SOPs, FDA regulations, and basic GCP requirements.
Qualification & Experience:
Minimum Education Required: High School Diploma or equivalent
Preferred Education: Clinical Medical Assistant, EMT, Paramedic, military medic with recent clinical experience, or higher
1-2 years of work experience in a clinical or research environment, or in a patient care setting; and
1-2 years of work experience in a role with phlebotomy responsibilities
Job ID: 514500113
Originally Posted on: 3/21/2026
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