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Clinical Operations Associate Jobs in Elmhurst, IL

ICON

Senior Clinical Research Associate

Chicago, IL · On-site +1

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Research Associate - Oncology - Midwest ICON is a global healthcare intelligence ... May serve as a subject matter expert for clinical operations on monitoring related activities (Sr ...

Icon plc

Senior Clinical Research Associate

Chicago, IL · On-site

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Research Associate - Oncology - Midwest ICON is a global healthcare intelligence ... May serve as a subject matter expert for clinical operations on monitoring related activities (Sr ...

PatientIQ

Strategy and Operations Associate

Chicago, IL · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... smarter clinical decisions and accelerating the future of value-based care. Headquartered in ... The opportunity PatientIQ is hiring a Strategy & Operations Associate to help drive the company ...

ChenMed, LLC

Associate Market Clinical Director

Oak Lawn, IL · On-site

$80K - $110K/yr

The Associate Market Clinical Director will directly supervise, performance manage and train ... Ensures successful clinical operations and meeting/exceeding plan market earnings. * Manages ...

Tempus

(Sr) Associate, Strategy & Operations

Chicago, IL · On-site

$70K - $85K/yr

  • Medical

  • Life

... clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of ... The (Sr)Associate - Sequencing Strategy & Operations role provides critical operational, analytical ...

Tempus

(Sr) Associate, Strategy & Operations

Chicago, IL

$70K - $85K/yr

  • Medical

  • Life

... clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of ... The (Sr)Associate - Sequencing Strategy & Operations role provides critical operational, analytical ...

ChenMed

Associate Market Clinical Director

Oak Lawn, IL · On-site

$80K - $110K/yr

The Associate Market Clinical Director will directly supervise, performance manage and train ... Ensures successful clinical operations and meeting/exceeding plan market earnings. * Manages ...

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Showing results 21-40

All JobsClinical Operations Associate JobsClinical Operations Associate Jobs in Elmhurst, IL

Clinical Operations Associate information

See Elmhurst, IL salary details

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How much do clinical operations associate jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for clinical operations associate in Elmhurst, IL is $26.14, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $30.14 per hour, depending on experience, location, and employer.

What is a clinical operations associate?

A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.

What are the typical responsibilities and team dynamics for a clinical operations associate?

As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

What are the key skills and qualifications needed to thrive in the clinical operations associate position, and why are they important?

To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.

What are the most commonly searched types of Clinical Operations jobs in Elmhurst, IL?

The most popular types of Clinical Operations jobs in Elmhurst, IL are:

What are popular job titles related to Clinical Operations Associate jobs in Elmhurst, IL?

For Clinical Operations Associate jobs in Elmhurst, IL, the most frequently searched job titles are:

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The top searched job categories for Clinical Operations Associate jobs in Elmhurst, IL are:

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Cities near Elmhurst, IL with the most Clinical Operations Associate job openings:

Clinical Operations Associate jobs near you
Infographic showing various Clinical Operations Associate job openings in Elmhurst, IL as of August 2026, with employment types broken down into 100% Full Time. Highlights an 92% In-person, and 8% Hybrid job distribution, with an average salary of $54,369 per year, or $26.1 per hour.

Senior Clinical Research Associate

ICON

Chicago, IL • On-site, Remote

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 19 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

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