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Assistant Clinical Project Manager Jobs in Illinois

... Clinical Teams, and Public Affairs). Applies knowledge across multiple therapeutic areas to support ... Appropriately advises management of project risks and presents recommendations for resolution.

... * Assist with study start up and oversee workload resourcing for team while providing primary ... Clinical Project Manager, III: Requires a bachelor's (or equivalency) + 6 years or a master's (or ...

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

... * Assist with study start up and oversee workload resourcing for team while providing primary ... Clinical Project Manager, III: Requires a bachelor's (or equivalency) + 6 years or a master's (or ...

... * Assist with study start up and oversee workload resourcing for team while providing primary ... Clinical Project Manager, III: Requires a bachelor's (or equivalency) + 6 years or a master's (or ...

... * Assist with study start up and oversee workload resourcing for team while providing primary ... Clinical Project Manager, III: Requires a bachelor's (or equivalency) + 6 years or a master's (or ...

Clinical Project Managers

Campus, IL ยท On-site

$125 - $150/hr

... * Assist with study start up and oversee workload resourcing for team while providing primary ... Clinical Project Manager, III : Requires a bachelor's (or equivalency) + 6 years or a master's (or ...

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Assistant Clinical Project Manager information

See Illinois salary details

$31K

$70.8K

$112.9K

How much do assistant clinical project manager jobs pay per year?

As of Sep 7, 2026, the average yearly pay for assistant clinical project manager in Illinois is $70,800.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,800.00 and $85,300.00 per year, depending on experience, location, and employer.

What is an assistant clinical project manager?

Assistant Clinical Project Managers are professionals who support the planning, coordination, and execution of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They work under the supervision of Clinical Project Managers to ensure that studies are conducted according to regulatory guidelines, timelines, and budgets. Their responsibilities often include tracking project progress, maintaining documentation, coordinating with cross-functional teams, and addressing issues that arise during clinical studies. This role is vital in ensuring that clinical projects run smoothly and efficiently, ultimately supporting the development of new medical treatments.

How does an assistant clinical project manager typically collaborate with cross-functional teams during a clinical trial?

An Assistant Clinical Project Manager works closely with various teams, including clinical research associates, regulatory affairs, data management, and quality assurance, to ensure successful trial execution. They often coordinate meetings, track project timelines, and facilitate communication between internal stakeholders and external vendors. This collaboration ensures that all regulatory requirements are met and that the study stays on schedule, making strong organizational and interpersonal skills essential for success in the role.

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

To thrive as an Assistant Clinical Project Manager, you need a solid understanding of clinical research processes, regulatory guidelines (such as GCP), and a relevant degree in life sciences or a related field. Familiarity with project management tools (like MS Project), clinical trial management systems (CTMS), and sometimes certifications such as PMP are valuable assets. Strong organizational, problem-solving, and interpersonal communication skills set candidates apart in this role. These skills and qualifications are critical for ensuring clinical trials run efficiently, compliantly, and collaboratively from start to finish.

What is the difference between Assistant Clinical Project Manager vs Clinical Project Manager?

AspectAssistant Clinical Project ManagerClinical Project Manager
CredentialsBachelor's degree, relevant certifications often preferredBachelor's or higher, certifications like PMP beneficial
Work EnvironmentSupports project teams, assists in coordinationLeads projects, oversees planning and execution
Employer & Industry UsagePharmaceutical, biotech, clinical research organizationsSame industries, higher responsibility
Search & Comparison IntentYesYes

The Assistant Clinical Project Manager typically supports the Clinical Project Manager by handling specific tasks and assisting in project coordination. The Clinical Project Manager holds a leadership role, overseeing the entire project lifecycle, making strategic decisions, and managing teams. Both roles are essential in clinical research, but the Assistant role is more entry-level and supportive, while the Clinical Project Manager has greater responsibility and authority.

What are the most commonly searched types of Clinical Project Manager jobs in Illinois?

The most popular types of Clinical Project Manager jobs in Illinois are:

What are popular job titles related to Assistant Clinical Project Manager jobs in Illinois?

For Assistant Clinical Project Manager jobs in Illinois, the most frequently searched job titles are:

What job categories do people searching Assistant Clinical Project Manager jobs in Illinois look for?

The top searched job categories for Assistant Clinical Project Manager jobs in Illinois are:

What cities in Illinois are hiring for Assistant Clinical Project Manager jobs?

Cities in Illinois with the most Assistant Clinical Project Manager job openings:

Infographic showing various Assistant Clinical Project Manager job openings in Illinois as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $70,800 per year, or $34 per hour.

Clinical Project Manager

Hematogenix Laboratory Sv

Tinley Park, IL โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 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.