1

Clinical Data Associate Jobs in Chicago, IL (NOW HIRING)

You will analyze and validate hospital-based clinical, supply, and physician data from multiple ... Mentor junior associates on procedural data concepts, validation approaches, and effective ...

Recruit, evaluate, onboard, mentor, and retain associate dentists * Review clinical performance data and create individualized improvement plans * Partner with operations and leadership to improve ...

New

Tempus is seeking a highly motivated Strategy & Operations Associate to join our Clinical Data Abstraction team. This role will support operational execution and process improvement for a large-scale ...

Tempus is seeking a highly motivated Strategy & Operations Associate to join our Clinical Data Abstraction team. This role will support operational execution and process improvement for a large-scale ...

next page

Showing results 1-20

Clinical Data Associate information

See Chicago, IL salary details

$14

$40

$89

How much do clinical data associate jobs pay per hour?

As of Jul 30, 2026, the average hourly pay for clinical data associate in Chicago, IL is $40.13, according to ZipRecruiter salary data. Most workers in this role earn between $30.19 and $40.10 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Data Associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

Which is better, CDM or SAS?

For a Clinical Data Associate, SAS is a widely used software for data analysis and reporting in clinical trials, while CDM (Clinical Data Management) refers to the overall process of collecting, cleaning, and managing clinical data, often using various tools including SAS. SAS skills are highly valued in the role, but understanding the broader CDM process is also important for effective data handling and compliance.

What's next after CRC?

After working as a Clinical Research Coordinator (CRC), professionals often advance to roles such as Clinical Data Associate, Clinical Trial Manager, or Regulatory Affairs Specialist. Gaining experience, certifications like CCRP, and developing skills in data management and regulatory compliance can facilitate career progression in clinical research.

What are the key skills and qualifications needed to thrive as a Clinical Data Associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What does a Clinical Data Associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What is the role of a clinical data associate?

A clinical data associate is responsible for collecting, managing, and ensuring the accuracy of data from clinical trials. They review data for completeness, resolve discrepancies, and use database tools to support data integrity and regulatory compliance throughout the trial process.

What Does a Clinical Data Associate Do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

Do you need a degree to be a CRC?

A Clinical Data Associate (CDA) typically does not require a specific degree, but a background in life sciences, healthcare, or related fields is often preferred. Many employers value relevant certifications and experience with clinical data management tools. Educational requirements can vary by employer and job level.

Is CRA an entry level job?

A Clinical Data Associate (CDA) role is typically considered an entry-level position in clinical research, often requiring a bachelor's degree in a related field and some familiarity with data management tools. However, a Clinical Research Associate (CRA) role usually requires more experience and is considered a mid- to senior-level position, involving site monitoring and regulatory compliance. Entry-level roles may serve as a stepping stone toward CRA positions with additional experience and certifications.

What is the difference between Clinical Data Associate vs Clinical Research Coordinator?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

What are the most commonly searched types of Clinical Data jobs in Chicago, IL? The most popular types of Clinical Data jobs in Chicago, IL are:
What are popular job titles related to Clinical Data Associate jobs in Chicago, IL? For Clinical Data Associate jobs in Chicago, IL, the most frequently searched job titles are:
What job categories do people searching Clinical Data Associate jobs in Chicago, IL look for? The top searched job categories for Clinical Data Associate jobs in Chicago, IL are:
What cities near Chicago, IL are hiring for Clinical Data Associate jobs? Cities near Chicago, IL with the most Clinical Data Associate job openings:
Infographic showing various Clinical Data Associate job openings in Chicago, IL as of July 2026, with employment types broken down into 1% As Needed, 72% Full Time, 25% Part Time, 1% Temporary, and 1% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $83,463 per year, or $40.1 per hour.

Senior Associate, Data Operations

Vizient, Inc.

Chicago, IL • On-site

$77K - $135K/yr

Other

Re-posted 20 days ago


Job description

When you're the best, we're the best. We instill an environment where employees feel engaged, satisfied and able to contribute their unique skills and talents while living and working as their authentic selves. We provide extensive opportunities for personal and professional development, building both employee competence and organizational capability to fuel exceptional performance through an inclusive environment both now and in the future.

Summary:


In this role, you will independently manage complex data intake, validation, and quality operations supporting Vizient's Procedural Analytics (PA) product. You will analyze and validate hospital-based clinical, supply, and physician data from multiple Electronic Medical Records (EMR) systems to ensure accuracy, completeness, and compliance with Vizient standards. You will collaborate with clients and internal partners to support implementations, resolve escalated data issues, and deliver high-quality analytic outputs. You will lead moderately complex projects, contribute to process improvements, and support enhancements to methodologies and training.

Responsibilities:

  • Execute complex procedural data implementations, including file intake, data mapping, normalization, and processing across multiple EMR-sourced datasets.
  • Perform advanced manual and automated data validation to identify mapping discrepancies, missing elements, integrity issues, and compliance gaps.
  • Ensure hospital submissions meet Vizient data quality standards across intake requirements, processing systems, and analytic outputs.
  • Serve as the primary escalation point for complex data issues, guiding members and internal teams through root cause analysis and resolution.
  • Diagnose and resolve ongoing submission issues, including intake failures, mapping errors, and data quality exceptions, coordinating solutions with internal and external stakeholders.
  • Monitor processing systems to confirm accurate data loading, availability, and readiness in PA tools.
  • Support development, testing, and rollout of new workflows, tools, and validation enhancements to improve data quality and efficiency.
  • Deliver customized analyses using structured and unstructured datasets to support PA benchmarking and insights.
  • Research and evaluate data sources, validation techniques, and best practices to continuously strengthen analytic and quality methodologies.
  • Translate complex data findings into clear, actionable recommendations for internal teams and member stakeholders.
  • Act as a trusted data advisor to members, providing guidance on methodology, data interpretation, and submission requirements.
  • Collaborate closely with project managers, engineers, and cross-functional partners to manage expectations and resolve data-related challenges.
  • Maintain accurate documentation and contribute to training materials that support standardized data intake, validation, and submission processes.
  • Mentor junior associates on procedural data concepts, validation approaches, and effective troubleshooting techniques.

Qualifications:

  • Relevant degree preferred.
  • 5 or more years of relevant experience required.
  • Strong SQL and Databricks skills, including querying complex relational databases and data troubleshooting required.
  • Advanced analytical skills with experience working with large, complex datasets using spreadsheet and data tools required.
  • Advanced, hands-on Excel skills required; candidates must be comfortable using LOOKUP functions, pivot tables, charts, and graphs on a daily basis.
  • Demonstrated ability to manage multiple priorities and projects in a high-volume operational environment required.
  • Clinical or perioperative background, including surgical nursing or equivalent experience, highly preferred.
  • Experience with perioperative data, OR workflows, surgical supplies, and preference cards preferred.
  • Experience with EMR systems such as Epic OpTime or Cerner SurgiNet preferred.
  • Experience supporting healthcare analytics platforms or benchmarking tools preferred.
  • Strong written and verbal communication skills with the ability to engage effectively with clients.

Estimated Hiring Range:

At Vizient, we consider skills, experience, and organizational needs in our compensation approach. Geographic factors may adjust the range estimate and hires typically fall below the top range. Compensation decisions are tailored to individual circumstances. The current salary range for this role is $77,400.00 to $135,400.00.

This position is also incentive eligible.

Vizient has a comprehensive benefits plan! Please view our benefits here:

http://www.vizientinc.com/about-us/careers

Equal Opportunity Employer: Females/Minorities/Veterans/Individuals with Disabilities

The Company is committed to equal employment opportunity to all employees and applicants without regard to race, religion, color, gender identity, ethnicity, age, national origin, sexual orientation, disability status, veteran status or any other category protected by applicable law.