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Clinical Project Manager Jobs in Bolingbrook, IL

CEDENT

Senior Clinical Project Manager

Chicago, IL

Biotech or Pharma company clinical operations experience in progressively responsible positions, including Senior/Clinical Project or Trial Manager * 7+ years' experience managing clinical trials ...

Deciphex Limited

Project Manager

Naperville, IL · On-site

  • Medical

  • PTO

Hands-on experience in histopathology, ideally with exposure to clinical trials and/or tissue biomarker studies * Demonstrable project management experience, bonus points if it's from a pharma ...

Deciphex

Project Manager

Naperville, IL · On-site

  • Medical

  • PTO

Hands-on experience in histopathology, ideally with exposure to clinical trials and/or tissue biomarker studies * Demonstrable project management experience, bonus points if it's from a pharma ...

Optimas Solutions

Project Manager

Wood Dale, IL · On-site

$100K - $111K/yr

The Project Manager is responsible for leading cross-functional initiatives that support Optimas' strategic priorities and operational objectives. This role partners closely with teams across ...

Optimas Solutions

Project Manager

Wood Dale, IL · On-site

$100K - $111K/yr

Project Manager - Strategic Initiatives Onsite: Wood Dale, IL Salary: $100,600.00 - $111,400.00 Position overview: The Project Manager is responsible for leading cross-functional initiatives that ...

Burwood Group, Inc

Project Manager

Oak Brook, IL · On-site +1

Company Description Inside our Project Management Office The Project Management Office (PMO) at Burwood Group, now part of Sikich, is a dynamic team of professionals dedicated to leading ...

Optimas Solutions

Project Manager

Wood Dale, IL · On-site

$100K - $111K/yr

Project Manager - Strategic Initiatives Onsite: Wood Dale, IL Salary: $100,600.00 - $111,400.00 Position overview: The Project Manager is responsible for leading cross-functional initiatives that ...

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Clinical Project Manager information

See Bolingbrook, IL salary details

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How much do clinical project manager jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical project manager in Bolingbrook, IL is $60.03, according to ZipRecruiter salary data. Most workers in this role earn between $41.83 and $70.34 per hour, depending on experience, location, and employer.

How much do clinical project managers earn?

Clinical project managers typically earn between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. Compensation may also include bonuses and benefits related to project scope and complexity.

What is the difference between Clinical Project Manager vs Clinical Research Associate?

AspectClinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMPUsually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors and sitesMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageFound in pharmaceutical, biotech, and CRO companies overseeing entire projectsPrimarily employed by CROs and sponsors to monitor trial sites

The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

What does a clinical project manager do?

A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.

What are the key skills and qualifications needed to thrive as a clinical project manager, and why are they important?

To thrive as a Clinical Project Manager, you need expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.

What does a clinical project manager do?

A Clinical Project Manager oversees the planning, execution, and completion of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They coordinate teams, manage budgets, timelines, and ensure that studies comply with regulatory standards and company protocols. Clinical Project Managers act as the main point of contact between sponsors, vendors, and clinical research sites, working to ensure that trials progress smoothly and data integrity is maintained. Their role is critical in bringing new therapies and treatments to market safely and efficiently.

What are some common challenges clinical project managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.
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What are the most commonly searched types of Clinical Project jobs in Bolingbrook, IL?

The most popular types of Clinical Project jobs in Bolingbrook, IL are:

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Clinical Project Manager jobs near you
Infographic showing various Clinical Project Manager job openings in Bolingbrook, IL as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $124,853 per year, or $60 per hour.

Clinical Project Manager

Hematogenix Laboratory Sv

Tinley Park, IL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 12 days ago

Job description

**Please note that this position requires you to be onsite at our Tinley Park, IL, USA location.


About Hematogenix

Want a job with greater meaning and higher purpose? Every day Hematogenix employees are warriors fighting a noble and global war on cancer. Helping patients every day, and helping partners every day – with our diagnostic and research services.

Hematogenix is looking for talented and highly motivated individuals to join our team. We offer a competitive benefit package and career development opportunities to help you achieve your highest professional and personal goals. We are eager to show you all we have to offer and how you can grow with us.

Hematogenix is a specialized contract research organization and clinical laboratory with a global presence. Our team of board-certified clinical, anatomic and research pathologists work in conjunction with top scientists from around the world to provide quality testing, consultation, and guidance for all aspects of the company’s pharma and diagnostic services.


Job Purpose:

The Project Manager is responsible for successful planning of global phase II/III registrational clinical trials, study start up activities, logistics set up and support, study sample and data query management, monitoring turnaround times, data reconciliation and close out activities. Includes but not limited to:

  • manage the scope of clinical trial projects, ensuring objectives, timelines, quality standards, and budgets constraints are fully met.
  • anticipate and respond to any challenges that may occur during the lifecycle of a project.
  • deliver excellent customer service to clients and other project stakeholders.
  • reports to Hematogenix Executive Team


Accountabilities/Work Activities:

Study Initiation

  • Participate in meetings with potential clients to fully understand a project’s objectives and timelines.

Planning & Design

  • Identify required activities of projects.
  • Contribute to the creation of a mutually agreed upon Scope of Work documents with Sponsors.
  • Liaison with Hematogenix SMEs to support complex biomarker projects
  • Create study specific Laboratory Manuals and maintain required regulatory documents.

Executing

  • Host in-house or remote initiation meetings with all project personnel to ensure participants understand their individual contributions, as well as overall study objectives and timelines.
  • Develop and train project team as clinical trial projects formally begin
  • Create and maintain study tracking documents to ensure timelines are adhered to as applicable to each specific study or Sponsor requirements.

Monitoring & Controlling

  • Continually monitor progress of projects
  • Ensure project supplies and resources are being adequately maintained.

Study Closing

  • Support all Close out activities depending on the scope of services as applicable to the study design or Sponsor’s requirements.
  • Participate in any Close Out Visits
  • Support study audits as needed.


Experience and Education

  • Minimum Bachelor of Science degree with experience in Clinical Laboratory Science
  • 2-3 years’ experience in Project Management supporting Phase II/III global clinical trials.


Skills and Qualifications

  • Knowledge of GCP/CAP/CLIA and clinical project management processes
  • Knowledge of global clinical research industry and associated regulations
  • Must be able to communicate effectively and persuasively, both verbally and in writing, with clients, all levels of in-house Hematogenix personnel, and other project stakeholders
  • Personal computer skills (Microsoft Word, Excel, Power Point, etc.)
  • Ability to ambulate throughout the office and laboratory.

Benefits we Offer:

  • Medical
  • Dental
  • Vison
  • Life
  • 401k
  • PTO
  • Competitive Salary

Contact Information:

jobs@hematogenix.com; www.hematogenix.com

Hematogenix provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.