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Clinical Research Project Manager Jobs in Romeoville, IL

Barrington James

Clinical Research Coordinator

Chicago, IL · On-site

$25 - $33.25/hr

Clinical Research Coordinator - 6 Month, Full Time Contract Chicago, IL A clinical research site in ... Experience in managing multiple studies or open to doing so * CCRC also preferred Urgent need ...

University of Chicago Library

Research Analyst

Chicago, IL · On-site

$28.85 - $38.46/hr

Supervises Clinical Research Coordinators. Responsibilities * Applies research principles and ... Project management. * Grant operations. * Database management. * Team leadership. * Participant ...

The University of Chicago

Research Analyst

Chicago, IL · On-site

$28.85 - $38.46/hr

Supervises Clinical Research Coordinators. Responsibilities * Applies research principles and ... Project management. * Grant operations. * Database management. * Team leadership. * Participant ...

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All JobsClinical Research Project JobsClinical Research Project Manager JobsClinical Research Project Manager Jobs in Romeoville, IL

Clinical Research Project Manager information

See Romeoville, IL salary details

$51K

$87.7K

$134.6K

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

As of Aug 7, 2026, the average yearly pay for clinical research project manager in Romeoville, IL is $87,718.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,900.00 and $93,300.00 per year, depending on experience, location, and employer.

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

AspectClinical Research Project ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in health sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, and liaises with sponsorsConducts daily clinical trial activities, interacts directly with participants and site staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch hospitals, clinics, academic institutions

The Clinical Research Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, ensuring protocol adherence and participant safety. Both roles are essential but differ in scope and responsibilities.

What does a clinical research project manager do?

A Clinical Research Project Manager oversees the planning, execution, and management of clinical research studies. They coordinate teams, ensure regulatory compliance, manage budgets and timelines, and act as a liaison between stakeholders such as sponsors, investigators, and regulatory agencies. Their primary goal is to ensure that clinical trials are conducted efficiently, ethically, and according to protocol. This role requires strong organizational, leadership, and communication skills, as well as a deep understanding of clinical research processes.

What are some common challenges faced by clinical research project managers and how can they be addressed?

Clinical Research Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance, and coordinating communication between diverse stakeholders. Balancing the needs of sponsors, research teams, and regulatory bodies requires strong organizational and problem-solving skills. Staying proactive with risk management and fostering clear, consistent communication can help address these challenges effectively. Leveraging project management tools and regularly scheduled check-ins also supports smoother project execution and team collaboration.

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

To thrive as a Clinical Research Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with tools such as CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications like PMP or ACRP-PM is highly valuable. Strong leadership, communication, and problem-solving skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial to ensure trials are conducted efficiently, ethically, and in line with regulatory standards.
What cities near Romeoville, IL are hiring for Clinical Research Project Manager jobs? Cities near Romeoville, IL with the most Clinical Research Project Manager job openings:
Clinical Research Project Manager jobs near you
Infographic showing various Clinical Research Project Manager job openings in Romeoville, IL as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $87,718 per year, or $42.2 per hour.

Clinical Research Coordinator

Genesis Orthopedics & Sports Medicine

Oak Brook, IL • On-site

$24.50 - $32.50/hr

Full-time

Re-posted 24 days ago

Job description

Genesis Orthopedics & Sports Medicine is seeking a motivated, organized, and detail-oriented Clinical Research Coordinator to join our growing research department in Oak Brook, Illinois. This is a full-time, on-site position (Monday through Friday, 40 hours per week) with opportunity for long-term growth within a rapidly expanding clinical research program.

We are looking for candidates with prior clinical research experience who thrive in a fast-paced environment, can independently manage multiple studies, and are passionate about patient care and advancing clinical research.

RESPONSIBILITIES

• Coordinate and manage clinical trials from study startup through closeout

• Independently manage 3 to 4 active studies simultaneously

• Recruit, screen, consent, and schedule study participants

• Conduct and support study visits in accordance with protocol requirements

• Perform accurate source documentation and timely data entry

• Enter and maintain study data within EDC systems

• Utilize IRT systems for patient randomization and drug accountability

• Maintain regulatory binders and essential study documents

• Assist with IRB submissions, regulatory maintenance, and study updates

• Communicate with sponsors, CROs, monitors, investigators, and patients

• Ensure protocol compliance, GCP adherence, and audit readiness

• Support patient retention and follow-up efforts

• Assist with lab processing, specimen handling, and shipment preparation as needed

Requirements

• Minimum 1 to 2 years of clinical research experience preferred

• Experience working on studies within the musculoskeletal (MSK) and cardiometabolic therapeutic areas preferred

• Ability to independently manage multiple studies and competing deadlines

• Phlebotomy trained and comfortable performing blood draws

• Experience using CRIO CTMS, eSource, and eRegulatory systems preferred

• Experience with EDC platforms and clinical trial data entry required

• Familiarity with IRT systems preferred

• Experience maintaining regulatory documentation and essential study files

• Strong understanding of GCP and clinical research workflows

• Excellent organizational, communication, and multitasking skills

• Ability to work independently and collaboratively within a team environment

• CRC certification is a plus but not required

• Medical assistant, nursing, healthcare, or research background preferred

Benefits

• Full-time, on-site position Monday through Friday

• Opportunity for professional growth and advancement

• Exposure to a variety of therapeutic areas and clinical trials

• Supportive and collaborative team environment

• Opportunity to grow within an expanding research program