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Clinical Research Program Manager Jobs in Northbrook, IL

Genesisortho

Clinical Research Coordinator

Oak Brook, IL · On-site

$55 - $75/hr

... 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 ...

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CVAUSA

Clinical Research Coordinator

Schaumburg, IL · On-site

$52 - $72/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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All JobsClinical Research Program JobsClinical Research Program Manager JobsClinical Research Program Manager Jobs in Northbrook, IL

Clinical Research Program Manager information

See Northbrook, IL salary details

$45.2K

$94K

$151.7K

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 Northbrook, IL is $93,991.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,600.00 and $106,600.00 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 Northbrook, IL?

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

What job categories do people searching Clinical Research Program Manager jobs in Northbrook, IL look for?

The top searched job categories for Clinical Research Program Manager jobs in Northbrook, IL are:

What cities near Northbrook, IL are hiring for Clinical Research Program Manager jobs?

Cities near Northbrook, IL with the most Clinical Research Program Manager job openings:

Clinical Research Program Manager jobs near you

Clinical Research Coordinator

Genesis Orthopedics & Sports Medicine

Oak Brook, IL • On-site

$24.50 - $32.50/hr

Full-time

Re-posted 22 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 

Apply