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Assistant Clinical Research Rater Jobs in Chicago, IL

Clinical Research Assistant

Lemont, IL · On-site

$21 - $23.50/hr

Position Summary We are now hiring for a Clinical Research Assistant that will support a high-volume Resarch Department within an ophthalmic practice that focuses on providing quality and ...

Clinical Research Coordinator

Lisle, IL

$24 - $31.75/hr

Conduct chart reviews and extract relevant clinical information to support research data collection. * Assist with patient recruitment activities in clinical and research settings. * Utilize ...

Clinical Research Coordinator

Lisle, IL

$24 - $31.75/hr

Conduct chart reviews and extract relevant clinical information to support research data collection. * Assist with patient recruitment activities in clinical and research settings. * Utilize ...

Clinical Research Coordinator Assistant

Chicago, IL · On-site

$25 - $33.25/hr

The Clinical Research Coordinator (CRC) Assistant will work collaboratively with a multi-institutional team. The CRC assistant will support the CRC, administrative staff and principal investigators ...

Clinical Research Coordinator Assistant

Chicago, IL · On-site

$25 - $33.25/hr

The Clinical Research Coordinator (CRC) Assistant will work collaboratively with a multi-institutional team. The CRC assistant will support the CRC, administrative staff and principal investigators ...

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Assistant Clinical Research Rater information

See Chicago, IL salary details

$11

$20

$29

How much do assistant clinical research rater jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for assistant clinical research rater in Chicago, IL is $20.84, according to ZipRecruiter salary data. Most workers in this role earn between $17.07 and $24.04 per hour, depending on experience, location, and employer.

What is the difference between Assistant Clinical Research Rater vs Clinical Research Coordinator?

AspectAssistant Clinical Research RaterClinical Research Coordinator
Required CredentialsHigh school diploma or equivalent; some roles may require a bachelor's degreeBachelor's degree in health sciences or related field; certification often preferred
Work EnvironmentRemote or in clinical settings; primarily data review and assessmentsClinical sites; managing study logistics and participant coordination
Employer & Industry UsageResearch organizations, pharmaceutical companies, universitiesHospitals, research institutions, pharmaceutical companies
Common Search & Comparison IntentUnderstanding entry-level roles in clinical researchManaging clinical trials and participant interactions

The Assistant Clinical Research Rater typically focuses on reviewing and assessing data, often working remotely, with minimal direct patient interaction. In contrast, the Clinical Research Coordinator manages the overall conduct of clinical trials, including participant recruitment and site management. Both roles are essential in clinical research but differ in responsibilities, required credentials, and work environment.

What are the most commonly searched types of Clinical Research Rater jobs in Chicago, IL? The most popular types of Clinical Research Rater jobs in Chicago, IL are:
Infographic showing various Assistant Clinical Research Rater job openings in Chicago, IL as of August 2026, with employment types broken down into 86% Full Time, 9% Part Time, and 5% Contract. Highlights an 100% In-person job distribution, with an average salary of $43,348 per year, or $20.8 per hour.

Unblinded Clinical Research Coordinator

DM Clinical Research

Chicago, IL

$25 - $33.25/hr

Full-time

Re-posted 5 days ago


Job description

Unblinded Clinical Research Coordinator
DM Clinical Research, the largest privately-owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties amp; Responsibilities:
  • Compound and dispense prescribed IP.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • Provide consultative support regarding the preparation and dosing of drugs.
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction.
  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials.
  • Understand and apply all applicable site procedures.
  • Ensure receipt and proper storage of IP and bioretention samples.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Foreign Medical Graduate is a plus
  • Pharmacy Technician Certification a plus
Experience:
  • Clinical Experience
Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)
Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred but not required