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Clinical Trial Rn Jobs in Illinois (NOW HIRING)

CVAUSA

Clinical Research Coordinator

Schaumburg, IL · On-site

$60 - $80/hr

As part of our expansion, we are increasing our clinical trial operations and are seeking dynamic ... Clinical experience in cardiovascular medicine in a clinical role (e.g., RN, technologist, medical ...

CVAUSA

Clinical Research Coordinator

Moline, IL · On-site

$60 - $80/hr

As part of our expansion, we are increasing our clinical trial operations and are seeking dynamic ... Clinical experience in cardiovascular medicine in a licensed role (e.g., RN, technologist, medical ...

AbbVie

Clinical Safety Analyst

North Chicago, IL · On-site +1

$65K/yr

Bachelor's degree with related health science background. RN or clinical pharmacy experience ... clinical trial life cycle management - Pre-clinical to Phase III through launch to market.

AbbVie

Clinical Safety Analyst

North Chicago, IL

Bachelor's degree with related health science background. RN or clinical pharmacy experience ... clinical trial life cycle management - Pre-clinical to Phase III through launch to market.

AbbVie

Clinical Safety Analyst

North Chicago, IL · On-site

Bachelor's degree with related health science background. RN or clinical pharmacy experience ... clinical trial life cycle management - Pre-clinical to Phase III through launch to market.

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Showing results 21-40

All JobsClinical Trial Rn JobsClinical Trial Rn Jobs in Illinois

Clinical Trial Rn information

See Illinois salary details

$27

$60

$93

How much do clinical trial rn jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for clinical trial rn in Illinois is $60.58, according to ZipRecruiter salary data. Most workers in this role earn between $49.13 and $68.27 per hour, depending on experience, location, and employer.

What is a Clinical Trial RN?

A Clinical Trial RN (Registered Nurse) is a specialized nurse who plays a key role in clinical research studies. They assist in patient recruitment, administer treatments, monitor patient responses, and ensure adherence to study protocols. They also collect and document data, work closely with principal investigators, and ensure compliance with regulatory guidelines. Their role is essential in advancing medical research and improving patient care through clinical trials.

What are the typical responsibilities of a Clinical Trial RN?

As a Clinical Trial RN, your daily tasks often involve screening and enrolling study participants, administering investigational treatments, monitoring patient responses, and accurately documenting all trial data. You will collaborate closely with physicians, research coordinators, and other healthcare professionals to ensure adherence to study protocols and patient safety guidelines. Additionally, you may educate patients and their families about trial procedures and follow up with them throughout the study. This role combines patient care with administrative and regulatory responsibilities, offering a dynamic and meaningful work environment.

What are the key skills and qualifications needed to thrive as a Clinical Trial RN?

To thrive as a Clinical Trial RN, you need a solid background in nursing practice, current RN licensure, and an understanding of clinical research protocols. Familiarity with clinical trial management systems, electronic data capture tools, and Good Clinical Practice (GCP) certification is often required. Strong attention to detail, superior organizational abilities, and effective communication skills make candidates excel in this role. These competencies are crucial to ensure patient safety, regulatory compliance, and the accurate collection and reporting of trial data.

How to get into clinical trial registered nurse?

To become a clinical trial registered nurse, you typically need to hold a valid registered nurse (RN) license, gain experience in medical or research settings, and obtain specialized training in clinical research protocols. Certification through organizations like the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) can enhance job prospects. Strong communication skills, attention to detail, and familiarity with Good Clinical Practice (GCP) guidelines are also important.

What do clinical trial RNs do in clinical trials?

Clinical trial RNs coordinate and monitor patient care during clinical studies, ensuring protocol adherence and accurate data collection. They perform assessments, administer treatments, educate participants, and document outcomes while following regulatory and safety guidelines.

What are popular job titles related to Clinical Trial Rn jobs in Illinois?

For Clinical Trial Rn jobs in Illinois, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Rn jobs in Illinois look for?

The top searched job categories for Clinical Trial Rn jobs in Illinois are:

Clinical Trial Rn jobs near you
Infographic showing various Clinical Trial Rn job openings in Illinois as of September 2026, with employment types broken down into 2% As Needed, 69% Full Time, 20% Part Time, 6% Contract, and 3% Nights. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $126,006 per year, or $60.6 per hour.

Clinical Independent Rater for Clinical Trial

IQVIA

Chicago, IL • Remote

Part-time

Posted 15 days ago

Key responsibilities

  • Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available.

  • Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring.

  • Participate in all required orientation, training, and calibration activities.

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

63rd of 226 rated it services

Job description

Clinical Independent Rater - Polish Speaking

Location: Remote/Virtual
Hours: Estimated 10-16 hours per month
Role: Clinical Specialist

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

Position Overview

The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation.

Key Responsibilities

  • Participate in all required orientation, training, and calibration activities.

  • Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available.

  • Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring.

  • Complete assigned tasks and rater interactions according to schedule.

  • Submit all required documentation accurately and on time.

Required Qualifications

  • Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.

  • Experience:

    • Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically MINI and MADRS).

    • Minimum 3 years of clinical experience with psychiatric populations.

    • Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research).

    • Experience in CNS trials preferred.

  • Skills:

    • Strong interpersonal and communication skills for professional interaction at all levels.

    • Excellent organizational skills, attention to detail, time management, and problem-solving ability.

    • Proficiency with Windows and Microsoft Office applications.

Language Requirement

Current openings require fluency in English and native-level proficiency in Polish.

#LI-DNP #LI-Remote #LI-HCPN

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is z104,600.00 - z194,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

Pay

Benefits

Hours and flexibility

Workplace

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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