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Clinical Informatics Manager Jobs in Elmhurst, IL

Clinical and Product Partnership:** Collaborate closely with product managers, designers ... Experience in healthcare, clinical informatics, or other highly regulated industries * Exposure to ...

Clinical and Product Partnership:** Collaborate closely with product managers, designers ... Experience in healthcare, clinical informatics, or other highly regulated industries * Exposure to ...

Clinical and Product Partnership:** Collaborate closely with product managers, designers ... Experience in healthcare, clinical informatics, or other highly regulated industries * Exposure to ...

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Clinical Informatics Manager information

See Elmhurst, IL salary details

$25

$49

$71

How much do clinical informatics manager jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical informatics manager in Elmhurst, IL is $49.06, according to ZipRecruiter salary data. Most workers in this role earn between $39.52 and $62.02 per hour, depending on experience, location, and employer.

What does a clinical informatics manager do?

A Clinical Informatics Manager oversees the implementation and optimization of health information systems to improve patient care and workflow efficiency. They serve as a liaison between clinical staff and IT teams, ensuring that electronic health records (EHR) and other digital tools support clinical needs. Their role includes training users, analyzing data for process improvements, and ensuring compliance with healthcare regulations. Strong leadership, technical expertise, and a deep understanding of clinical workflows are essential for success in this position.

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

To thrive as a Clinical Informatics Manager, you need a solid background in healthcare, informatics, and project management, often supported by degrees in health informatics, nursing, or a related field, plus relevant experience. Familiarity with electronic health record (EHR) systems, data analytics tools, and industry certifications such as Certified Professional in Healthcare Information and Management Systems (CPHIMS) are commonly required. Excellent leadership, communication, and problem-solving skills enable success in managing interdisciplinary teams and driving technology adoption. These skills and qualifications are crucial for effectively aligning clinical workflows with technological solutions to improve patient care and organizational efficiency.

What can I do with a clinical informatics manager degree?

A clinical informatics manager oversees the implementation and management of healthcare information systems, improving clinical workflows and patient care. They often work with electronic health records (EHRs), data analysis, and health IT tools, requiring knowledge of healthcare regulations and certifications like CPHIMS or CAHIMS. This role typically involves leadership, project management, and collaboration with clinical staff and IT teams.

What are the most commonly searched types of Clinical Informatics jobs in Elmhurst, IL?

The most popular types of Clinical Informatics jobs in Elmhurst, IL are:

What job categories do people searching Clinical Informatics Manager jobs in Elmhurst, IL look for?

The top searched job categories for Clinical Informatics Manager jobs in Elmhurst, IL are:

What cities near Elmhurst, IL are hiring for Clinical Informatics Manager jobs?

Cities near Elmhurst, IL with the most Clinical Informatics Manager job openings:

Infographic showing various Clinical Informatics Manager job openings in Elmhurst, IL as of August 2026, with employment types broken down into 83% Full Time, 16% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $102,047 per year, or $49.1 per hour.

(Senior) Clinical Study Manager, Clinical Development

Tempus

Chicago, IL

$100K - $140K/yr

Full-time

Re-posted 11 days ago


Key responsibilities

  • Lead the planning, execution, and management of prospective and retrospective clinical studies.

  • Develop study protocols, Informed Consent Forms, Case Report Forms, and study-specific manuals.

  • Oversee vendor and site management, including site identification, feasibility assessments, and maintaining relationships with Principal Investigators.


Job description

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

We are seeking a highly motivated and detail-oriented Senior Clinical Study Manager (CSM) to join our Clinical Development team. In this role, you will lead the planning, execution, and management of both prospective and retrospective clinical evidence generation studies.

The ideal candidate thrives at the intersection of oncology, genomics, and data science. You will be responsible for ensuring that clinical studies are conducted with the highest quality standards, on time, and within budget, while leveraging Tempus's unique multimodal data platform.

Key Responsibilities

  • Study Leadership: Lead the end-to-end management of multiple clinical studies, including prospective observational trials and retrospective Real-World Evidence (RWE) studies.

  • Operational Planning: Develop study protocols, Informed Consent Forms (ICFs), Case Report Forms (CRFs), and study-specific manuals.

  • Vendor & Site Management: Oversee CROs, central labs, and clinical trial sites. Conduct site identification, feasibility assessments, and maintain strong relationships with Principal Investigators.

  • Data Integrity: Partner with Data Science and Bio-informatics teams to ensure high-quality data collection and clean datasets for retrospective analysis.

  • Compliance: Ensure all study activities adhere to ICH-GCP guidelines, HIPAA regulations, and internal Standard Operating Procedures (SOPs).

  • Cross-functional Collaboration: Work closely with Medical Affairs, Product, Legal, and Engineering teams to align study objectives with company milestones.

  • Timeline & Budget Tracking: Manage study milestones, identify potential risks to timelines, and implement mitigation strategies to keep projects on track.

Qualifications

  • Education: Bachelor's degree in a Life Sciences, Nursing, or related field (Advanced degree such as MS, MPH, or PhD preferred).

  • Experience: 5+ years of clinical trial management experience within a Biotech, Pharma, or CRO environment.

  • Domain Expertise: Strong understanding of oncology and/or molecular diagnostics. Experience with Real-World Data (RWD) or retrospective cohort studies is highly desirable.

  • Technical Skills: Proficiency with EDC systems, CTMS, and eTMF platforms. Familiarity with SQL or data visualization tools is a plus.

  • Soft Skills: Exceptional project management, communication, and problem-solving skills. Ability to work in a fast-paced, "startup" environment.

#LI-NK1

$100,000 - $140,000


The expected salary range may vary for other locations. Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.