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Clinical Research Program Manager Jobs in Illinois

CVAUSA

Clinical Research Coordinator

Moline, IL · On-site

$55 - $75/hr

... program while collaborating with clinic staff on existing and new clinical trials. As part of ... You will have the opportunity to manage your studies with a high degree of autonomy while working ...

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Clinical Research Program Manager information

See Illinois salary details

$43.1K

$89.7K

$144.9K

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

As of Sep 3, 2026, the average yearly pay for clinical research program manager in Illinois is $89,735.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,300.00 and $101,700.00 per year, depending on experience, location, and employer.

What does a clinical research program manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

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

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.

What are some typical challenges faced by clinical research program managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

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

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

What are popular job titles related to Clinical Research Program Manager jobs in Illinois?

For Clinical Research Program Manager jobs in Illinois, the most frequently searched job titles are:

What job categories do people searching Clinical Research Program Manager jobs in Illinois look for?

The top searched job categories for Clinical Research Program Manager jobs in Illinois are:

What cities in Illinois are hiring for Clinical Research Program Manager jobs?

Cities in Illinois with the most Clinical Research Program Manager job openings:

Clinical Research Program Manager jobs near you
Infographic showing various Clinical Research Program Manager job openings in Illinois as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 21% Part Time, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $89,735 per year, or $43.1 per hour.

Clinical Research Coordinator

Cardiovascular-Associates-of-America

Moline, IL • On-site

$52 - $76/hr

Other

Posted 19 days ago

Job description

Clinical Research Coordinator


Location: Moline Illinois


Job Type: Full-time


This is an onsite position in Moline, Illinois

About CVAUSA


Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to advancing medical research and improving patient outcomes. As part of our expansion, we are increasing our clinical trial operations and are seeking dynamic, results‑driven professionals to join our team.


At CVAUSA, we are focused on innovation and excellence in cardiovascular research, and we believe the best results come from individuals who are passionate about making a difference.


The Clinical Research Coordinator will be responsible for supporting the growth and development of the research program while collaborating with clinic staff on existing and new clinical trials. As part of CVAUSA’s national network, this role offers the opportunity to collaborate with teams across the country and make an impact both locally and nationwide.


Position Overview

As a Clinical Research Coordinator, you will play a key role in coordinating and overseeing clinical trials and supporting site operations. You will have the opportunity to manage your studies with a high degree of autonomy while working closely with investigators, sponsors, and site staff. This is an excellent opportunity for a motivated, detail-oriented individual who thrives in a fast‑paced environment.


Key Responsibilities
Clinical Trial Coordination

Coordinate all aspects of clinical trials, including patient recruitment, screening, enrollment, and follow-up visits. Ensure study protocols are followed accurately and consistently.


Site Operations

Support day-to-day research site operations while ensuring compliance with regulatory requirements and study protocols.


Data Management

Collect, verify, and maintain clinical trial data, ensuring accuracy, completeness, and timely entry.


Communication & Reporting

Serve as a primary point of contact for study sponsors, participants, and research stakeholders. Provide regular study updates and assist with reporting requirements.


Regulatory Compliance

Maintain up-to-date study documentation, regulatory binders, and patient records in compliance with GCP, ICH guidelines, and applicable regulations.


Process Improvement

Assist with identifying opportunities to improve research workflows and enhance study performance.


What We’re Looking For
Detail-Oriented & Organized

Able to manage multiple priorities while maintaining a high level of accuracy and quality.


Strong Communicator

Effectively communicates with sponsors, investigators, site staff, and participants.


Collaborative Team Player

Works well independently and as part of a multidisciplinary team.


Adaptable & Results-Oriented

Thrives in a dynamic environment and remains focused on achieving study goals.


Experience & Qualifications

  • Clinical experience in cardiovascular medicine in a licensed role (e.g., RN, technologist, medical assistant, etc.)

  • Bachelor’s degree in a relevant field (life sciences, healthcare, or clinical research) preferred

  • Minimum of 1–2 years of clinical research experience, including patient enrollment and study coordination

  • Strong organizational and time management skills

  • Clinical research certification (e.g., CCRP) preferred

  • Knowledge of GCP, ICH guidelines, and regulatory requirements

  • Experience with electronic data capture systems and regulatory documentation preferred


Why CVAUSA?

At CVAUSA, we believe in the power of innovation and are looking for professionals eager to make an impact in cardiovascular research. As part of our growing organization, you’ll be at the forefront of cutting‑edge clinical trials.

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