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Clinical Risk Manager Jobs in Aurora, IL (NOW HIRING)

IQVIA

Senior Global Clinical Study Manager

Chicago, IL · On-site

Drive global clinical trials from first site activation to final patient visit-own the strategy ... Develop and manage integrated study plans and risk mitigation strategies * Proactively identify ...

LifeStance Health

Clinical Director

Oswego, IL · On-site

$90K - $115K/yr

The Clinical Director ensures clinical integrity and compliance through local monitoring and risk management. Compensation: $90,000 - 115,000/annually, plus annual bonus potential Duties ...

LifeStance Health

Clinical Director

Aurora, IL · On-site

$90K - $115K/yr

The Clinical Director ensures clinical integrity and compliance through local monitoring and risk management. Compensation: $90,000 - 115,000/annually, plus annual bonus potential Duties ...

CEDENT

Senior Clinical Project Manager

Chicago, IL · On-site

Excellent communication (oral and/or written), leadership, and risk mitigation skills plus a ... Proven ability to effectively manage internal and external personnel in clinical trial conduct ...

Heartflow

Clinical Trial Manager

Chicago, IL · On-site

$95K - $125K/yr

The Clinical Trial Manager (CTM) is responsible for the oversight and management of all clinical ... risk mitigation, and contingency plans * Participates in and leads process improvement activities ...

Chicago Family Health Center

Clinical Nurse

Chicago, IL · On-site

$30 - $44/hr

Initiates the development of a care plan for each patient, which includes performing a risk ... Oversees care for management of multiple disease processes for diagnosed patients. * Provides ...

ConvaTec

Clinical Strategy Lead

Chicago, IL · On-site +1

... risk management, and other activities as needed. * Act as a subject matter expert in the product ... Clinical background (MD, RN, DPM, DNP, or similar) r equired * Specialty knowledge in wound care ...

Advocate Aurora Health

Claims Mgr

Oak Brook, IL · Hybrid

$47.50 - $71.25/hr

Analyzes and presents the Risk Management Annual Report summary and analysis to site executives, leaders, medical staff, clinical divisions and governing council. Reviews, analyzes, and develops ...

CONVATEC GROUP PLC

Clinical Strategy Lead

Chicago, IL · On-site +1

... risk management, and other activities as needed. * Act as a subject matter expert in the product ... Clinical background (MD, RN, DPM, DNP, or similar) r equired * Specialty knowledge in wound care ...

Friend Health

HRDI Clinical Supervisor ACT

Chicago, IL · On-site

$50K/yr

... risk management plans, the provision of offsite individual, group, and family therapy and the provision of assistance with placement of clients within the community. JOB DUTIES: * Provides clinical ...

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All JobsClinical Risk JobsClinical Risk Manager JobsClinical Risk Manager Jobs in Aurora, IL

Clinical Risk Manager information

See Aurora, IL salary details

$78K

$104.3K

$136.9K

How much do clinical risk manager jobs pay per year?

As of Aug 7, 2026, the average yearly pay for clinical risk manager in Aurora, IL is $104,313.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,203.00 and $126,701.00 per year, depending on experience, location, and employer.

How does a clinical risk manager collaborate with clinical staff to improve patient safety?

Clinical Risk Managers work closely with nurses, physicians, and other healthcare professionals to identify potential risks and prevent adverse events. They often conduct root cause analyses after incidents, facilitate safety training sessions, and lead multidisciplinary meetings to discuss risk mitigation strategies. By fostering open communication and encouraging reporting of near-misses, they help create a culture of safety and continuous improvement within the healthcare facility.

How to become a clinical risk manager?

To become a clinical risk manager, individuals typically need a bachelor's degree in nursing, healthcare administration, or a related field, followed by relevant work experience in healthcare settings. Many pursue certifications such as the Certified Professional in Healthcare Risk Management (CPHRM) to enhance their credentials. Strong knowledge of healthcare regulations, risk assessment skills, and the ability to analyze clinical data are essential for success in this role.

What do clinical risk managers do?

Clinical risk managers are responsible for identifying, assessing, and reducing risks related to patient safety and healthcare quality within medical facilities. They analyze incident reports, develop safety protocols, and ensure compliance with healthcare regulations, often using data analysis tools and requiring relevant certifications. Their goal is to minimize adverse events and improve overall clinical outcomes.

What are the key skills and qualifications needed to thrive as a clinical risk manager?

To thrive as a Clinical Risk Manager, you need a solid background in healthcare, risk management, and regulatory compliance, typically supported by a clinical degree and certifications such as CPHRM (Certified Professional in Healthcare Risk Management). Familiarity with incident reporting systems, electronic health records, and risk analysis tools is essential. Strong analytical thinking, communication, and problem-solving skills enable effective collaboration with healthcare teams and leadership. These competencies are vital for identifying, mitigating, and preventing risks to ensure patient safety and regulatory compliance in healthcare organizations.

What is the difference between Clinical Risk Manager vs Clinical Risk Coordinator?

AspectClinical Risk ManagerClinical Risk Coordinator
CertificationsCPHRM, RACCPHRM, RAC (sometimes)
Work EnvironmentHospitals, healthcare organizations, risk management departmentsClinics, healthcare facilities, risk management teams
ResponsibilitiesOversees risk management programs, develops policies, analyzes risksAssists in risk assessments, supports risk mitigation efforts, data collection

The Clinical Risk Manager typically holds more advanced certifications and has broader responsibilities in developing and overseeing risk management strategies. The Clinical Risk Coordinator supports these efforts through data collection and risk assessment assistance. Both roles are essential in healthcare risk management but differ in scope and seniority.

What are popular job titles related to Clinical Risk Manager jobs in Aurora, IL? For Clinical Risk Manager jobs in Aurora, IL, the most frequently searched job titles are:
What job categories do people searching Clinical Risk Manager jobs in Aurora, IL look for? The top searched job categories for Clinical Risk Manager jobs in Aurora, IL are:
What cities near Aurora, IL are hiring for Clinical Risk Manager jobs? Cities near Aurora, IL with the most Clinical Risk Manager job openings:
Clinical Risk Manager jobs near you
Infographic showing various Clinical Risk Manager job openings in Aurora, IL as of August 2026, with employment types broken down into 86% Full Time, 11% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $104,313 per year, or $50.2 per hour.

Senior Global Clinical Study Manager

IQVIA

Chicago, IL • On-site

Full-time

Re-posted 12 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 223 rated it services

Job description

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide.

Required Experience
  • 2+ years of global study management experience
  • Experience across multiple countries/regions
  • Phase I-III clinical trials experience (Phase III required)
  • Oncology experience required
  • Ability to work across multiple therapeutic areas
Job Overview

We are seeking a Global Study Manager responsible for the end-to-end planning, execution, and delivery of clinical trial site management activities across global studies. This role ensures successful site selection, activation, monitoring oversight, and closeout-while balancing speed, quality, and cost. You will serve as the primary point of contact for clients, lead cross-functional teams, and ensure compliance with ICH-GCP, regulatory requirements, and study protocols. This is a highly visible role that combines strategic leadership, operational execution, and financial oversight.

Key ResponsibilitiesGlobal Study & Site Leadership
  • Lead site management strategy from study award through close-out
  • Oversee site identification, selection, activation, and recruitment performance
  • Ensure clinical monitoring processes meet study needs and timelines
  • Partner with CRAs to optimize enrollment, data quality, and compliance
Project & Stakeholder Management
  • Serve as primary client contact and own key customer relationships
  • Lead cross-functional teams across regions and cultures
  • Facilitate internal and external meetings, including executive presentations
  • Drive collaboration across stakeholders, vendors, and functional leads
Operational Excellence & Risk Management
  • Develop and manage integrated study plans and risk mitigation strategies
  • Proactively identify risks and implement corrective/preventative actions
  • Monitor study timelines, enrollment trends, and data quality metrics
  • Ensure compliance with GCP, SOPs, protocols, and regulatory standards
Financial & Contract Management
  • Manage study financials, including forecasting and revenue acceleration
  • Identify and manage out-of-scope work and change orders
  • Oversee Billing Unit Reviews (BURs) and expense approvals
  • Track performance against budget and Estimate at Completion (EAC)
Quality & Compliance
  • Maintain TMF health and ensure timely document submission
  • Develop quality monitoring plans and compliance metrics
  • Ensure adherence to study tools, training materials, and processes
Team Leadership & Development
  • Lead and mentor cross-functional project teams
  • Support CRA and team training on therapeutic areas and study-specific needs
  • Foster collaboration, knowledge sharing, and continuous improvement
QualificationsRequired
  • Bachelor's degree in life sciences or related field
  • 5+ years of clinical research/monitoring experience, including 2 years in a clinical study management role
  • Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes
  • Experience managing global clinical trials and multi-regional teams
  • Demonstrated experience in project financial management
Core Competencies
  • Exceptional communication and stakeholder management skills
  • Strong problem-solving and risk mitigation capabilities
  • Ability to influence without authority in matrix organizations
  • High attention to detail and quality-driven mindset
  • Proficiency in Microsoft Office and clinical systems (e.g., CTMS, EDC)
Why Join Us
  • Work on cutting-edge global trials across therapeutic areas
  • Collaborate with top talent in a dynamic, global environment
  • Make a direct impact on patient outcomes worldwide

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 athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

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 $93,100.00 - $232,800.00. 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

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Hours and flexibility

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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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