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Research Associate Jobs in Addison, IL (NOW HIRING)

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Senior Clinical Research Associate

Chicago, IL · On-site

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Midwest ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

ICON

Senior Clinical Research Associate

Chicago, IL · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Midwest ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Alira Health

Clinical Research Associate

Geneva, IL

Summary ROLE The Clinical Research Associate is an important member of the Alira Health Clinical team. CRAs are highly motivated and function independently to conduct site monitoring responsibilities ...

ZS

Market Research Associate Consultant

Evanston, IL · On-site

$120K - $137K/yr

Strategy Insights and Planning Associate Consultant ZS's Strategy Insights and Planning teams ... Our recommendations and solutions are based on rigorous research and analysis underpinned by deep ...

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Research Associate information

See Addison, IL salary details

$16

$32

$46

How much do research associate jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for research associate in Addison, IL is $32.60, according to ZipRecruiter salary data. Most workers in this role earn between $26.25 and $37.07 per hour, depending on experience, location, and employer.

What is a research associate?

Research Associates are professionals who support research projects in academic, scientific, or business settings. They assist with designing studies, collecting and analyzing data, and preparing reports or publications. Research Associates often work under the supervision of principal investigators or senior researchers, contributing their expertise to advance the goals of the project. Their responsibilities can vary depending on the field, but typically involve both administrative and hands-on research tasks.

What does a research associate do?

As a research associate, you conduct research and analysis as directed by a senior researcher or project manager. Researchers work in a number of fields, including medical science, the social sciences, natural sciences, finance, management, and academia. Your specific duties and responsibilities differ depending on the field in which you work, but some features of your work are similar across industries. You typically do primary and secondary source research, organize and process data, analyze said data, and report on your findings to lead researchers or clinicians.

What are the key skills and qualifications needed to thrive as a research associate, and why are they important?

To thrive as a Research Associate, you need a strong background in research methodology, data analysis, and subject-specific knowledge, typically supported by a relevant bachelor's or master's degree. Familiarity with statistical software (such as SPSS, R, or Python), laboratory equipment, and research databases is often essential. Attention to detail, critical thinking, and clear written and verbal communication skills set outstanding Research Associates apart. These skills ensure accurate data collection, effective collaboration, and the production of reliable, impactful research outcomes.

What are some typical challenges a research associate might face when managing multiple research projects simultaneously?

As a Research Associate, juggling multiple projects often requires strong organizational skills and the ability to prioritize tasks effectively. You might encounter challenges such as balancing deadlines, coordinating with various team members, and adapting to shifting project goals or data requirements. Effective communication and proactive time management are essential to ensure each project progresses smoothly and meets its milestones. Many teams use project management tools and regular check-ins to help mitigate these challenges and support collaboration.

What is the difference between Research Associate vs Research Scientist?

AspectResearch AssociateResearch Scientist
Required CredentialsBachelor's or Master's degree in relevant fieldMaster's or PhD in relevant field
Work EnvironmentLaboratories, research institutions, universitiesLaboratories, research institutions, industry settings
Employer & Industry UsageAcademic, government, non-profitAcademic, industry, biotech, pharma
Common Search & ComparisonYesYes

The main difference between a Research Associate and a Research Scientist lies in their educational requirements and level of experience. Research Associates typically hold a bachelor's or master's degree and assist in research projects, while Research Scientists usually have a PhD and lead research efforts. Both roles work in similar environments like labs and research institutions, but Research Scientists often have more independence and responsibility.

What qualifications do you need to be a research associate?

Research associates typically need a bachelor's degree in a relevant field such as science, engineering, or social sciences. Many positions prefer or require a master's degree or higher, along with strong analytical skills, proficiency with research tools, and experience in data collection and analysis.
More about Research Associate jobs

What are the most commonly searched types of Research jobs in Addison, IL?

The most popular types of Research jobs in Addison, IL are:

What job categories do people searching Research Associate jobs in Addison, IL look for?

The top searched job categories for Research Associate jobs in Addison, IL are:

What cities near Addison, IL are hiring for Research Associate jobs?

Cities near Addison, IL with the most Research Associate job openings:

Research Associate jobs near you
Infographic showing various Research Associate job openings in Addison, IL as of September 2026, with employment types broken down into 1% As Needed, 67% Full Time, 29% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $67,812 per year, or $32.6 per hour.

Senior Clinical Research Associate

Chicago, IL

410 ICR United States USA
See more jobs at 410 ICR United States USAexternal

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 27 days ago

Job description

Senior Clinical Research Associate - Oncology - Midwest

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


What you will be doing:

  • Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and Internation Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines. 

  • Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and closes clinical trials at investigative sites. 

  • Responsible for site startup activities for assigned sites, including but not limited to regulatory documents collection, informed consent review, IRB/IEC submission support, and budgets and contracts negotiations. 

  • Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely

  • Provides regular site status information to team members, trial management, and updates trial management tools.

  • Completes monitoring activity documents as required by sponsor's SOPs.

  • Works closely with other clinical team members to facilitate timely resolution of trial and/or clinical issues.

  • Escalates site and trial related issues per Sponsor's SOPs until identified issues are resolved or closed.

  • Performs essential document site file reconciliation. 

  • Performs source document verification and query resolution. 

  • Assesses investigational product (IP) accountability, dispensation, and compliance at the investigative sites. 

  • Verifies serious adverse event (SAE) reporting according to trial specifications and ICH GCP guidelines.

  • Communicates with investigative sites.

  • Updates applicable tracking systems

  • Ensures all required training is completed and documented. 

  • Functions with little oversight (Sr level) 

  • May serve as a subject matter expert for clinical operations on monitoring related activities (Sr level)

  • May be assigned to complex studies and/or sites.

  • Provides leadership skills to assigned projects within the clinical operations department.

What you need to have:

  • Highly responsive and proactive, team player

  • An undergraduate degree or it’s equivalent in clinical, science, or health related field from an accredited institution; a licensed health care professional (i.e. registered nurse) or equivalent work experience required.

  • 5+ years clinical monitoring experience required (Sr CRA)

  • Knowledge of ICH and local regulatory authority regulations regarding drug

  • Read, write and speak fluent English.

  • Oncology Phase II/III monitoring experience required

  • Serves as observation and performance visit leader.

  • Experience doing feasibility/site selection/site start up required.

  • Budget negotiations experience preferred. 

  • May serve as a resource for and interact with other functional areas to resolve site issues and facilitate trial timelines.

  • May be assigned clinical tasks where advanced negotiating skills are required.

  • To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Salary Range

$110,520.00-$138,150.00

Are you a current ICON Employee? Please click here to apply