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

NEUROHEALTH ASSOCIATES PC

Psychologist

Oak Brook, IL · On-site

At NeuroHealth Associates, we practice precision mental health, integrating neuropsychological ... let data drive every clinical decision. You will be trained to interpret quantitative EEG (qEEG ...

ICON

CRA II and Senior CRA

Downers Grove, IL · On-site

$91K - $114K/yr

We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and ... Performing data review and resolution of queries to maintain high-quality clinical data.

Icon plc

CRA II and Senior CRA

Downers Grove, IL · Remote

$91K - $114K/yr

We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and ... Performing data review and resolution of queries to maintain high-quality clinical data.

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Romeoville, IL

Clinical Data Associate information

See Romeoville, IL salary details

$14

$39

$88

How much do clinical data associate jobs pay per hour?

As of Jul 18, 2026, the average hourly pay for clinical data associate in Romeoville, IL is $39.72, according to ZipRecruiter salary data. Most workers in this role earn between $29.90 and $39.71 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.

More about Clinical Data Associate jobs
What are the most commonly searched types of Clinical Data jobs in Romeoville, IL? The most popular types of Clinical Data jobs in Romeoville, IL are:
What job categories do people searching Clinical Data Associate jobs in Romeoville, IL look for? The top searched job categories for Clinical Data Associate jobs in Romeoville, IL are:
What cities near Romeoville, IL are hiring for Clinical Data Associate jobs? Cities near Romeoville, IL with the most Clinical Data Associate job openings:
Clinical Data Associate jobs near you

Psychiatric Mental Health Nurse Practitioner

NEUROHEALTH ASSOCIATES PC

Oak Brook, IL • On-site

Full-time

Posted 22 days ago

Job description

About the Role:
Join NEUROHEALTH ASSOCIATES PC as a Psychiatric Mental Health Nurse Practitioner, where you'll play a vital role in providing compassionate, evidence-based mental health care. Be part of a dedicated team in Oak Brook, IL, committed to improving the lives of our patients through innovative treatment approaches.

This is not a traditional medication management role.

At NeuroHealth Associates, we practice precision mental health, integrating neuropsychological testing, neurofeedback, pharmacology, and advanced biomarker testing to treat the causes of brain circuitry dysfunction, not just the symptoms. We are looking for a prescriber who shares this perspective: someone who's curious about the biology underlying the diagnosis and who lets data guide every clinical decision.
You will be trained to interpret quantitative EEG (qEEG) brain maps and use the information to inform your prescribing, protocols, and conversations with patients. If you have ever felt boxed in by 15-minute med checks and want to practice at the full depth of your clinical expertise, this is the practice you have been looking for.

What You Will Do
•     Interpret qEEG brain maps (full training provided) and understand neuropsychological test data, and use that data to inform every clinical decision.
•     Work closely with patients and families to monitor progress in neurofeedback protocols, with training to adjust those protocols based on clinical data and treatment response.
•     Provide supportive, time-limited consultations using structured modules, offering meaningful clinical contact without the burden of a traditional therapy caseload.
•     Utilize pharmacogenomic testing, organic acids panels, and specialized biomarker labs to identify the biological underpinnings driving brain circuitry dysfunction, because we treat causes, not just symptoms.
•     Review comprehensive neuropsychological test data with patients, track progress over time, and deepen your clinical expertise in ways most prescribers never get the opportunity to.

What You Will Bring
•     Active licensure as a Psychiatric Mental Health Nurse Practitioner (PMHNP) in Illinois
•     Prescriptive authority and DEA registration
•     A genuine curiosity about the biological drivers of mental health and a desire to practice data-informed, root-cause care.
•     Strong collaboration skills and authentic care for both patients and colleagues.

What We Offer
•     A precision mental health model you will not find at a conventional practice.
•     Hands-on training in qEEG interpretation, neurofeedback protocols, and advanced diagnostics
•     Flexible scheduling and telehealth options.
•     Full-time and part-time arrangements. We will build the right fit together.
•     Productivity-based compensation with strong earning potential as the practice grows.
•     A collaborative team built on respect and genuine care for both patients and staff.

Ready to Practice Differently?
If this sounds like the kind of work you have been looking for, we want to hear from you. Apply through this posting.