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Clinical Data Associate Jobs in Nebraska (NOW HIRING)

Heartland Family Service

Associate Clinical Director

Omaha, NE · On-site

$76K - $104K/yr

SUMMARY DESCRIPTION OF WORK The Associate Clinical Director (ACD) is a senior clinical leadership ... Utilizes clinical data to enhance client outcomes for therapists. * Experience in adult and child ...

Heartland Family Service

Associate Clinical Director

Omaha, NE · On-site

$76K - $104K/yr

SUMMARY DESCRIPTION OF WORK The Associate Clinical Director (ACD) is a senior clinical leadership ... Utilizes clinical data to enhance client outcomes for therapists. * Experience in adult and child ...

Heartland Family Service

Associate Clinical Director

Omaha, NE · On-site

$76K - $104K/yr

SUMMARY DESCRIPTION OF WORK The Associate Clinical Director (ACD) is a senior clinical leadership ... Utilizes clinical data to enhance client outcomes for therapists. * Experience in adult and child ...

Bryan Health

Clinical Quality Analyst

Lincoln, NE · On-site

Performs data analysis using multiple methods to identify trends, gaps, and opportunities for ... Associate's degree in Nursing, Health Information Management, Public Health, Healthcare ...

Bryan Health

Clinical Quality Analyst

Lincoln, NE · On-site

Performs data analysis using multiple methods to identify trends, gaps, and opportunities for ... Associate's degree in Nursing, Health Information Management, Public Health, Healthcare ...

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Clinical Data Associate information

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$13

$37

$82

How much do clinical data associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical data associate in Nebraska is $37.14, according to ZipRecruiter salary data. Most workers in this role earn between $27.98 and $37.12 per hour, depending on experience, location, and employer.

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 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.

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 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.

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 Nebraska?

The most popular types of Clinical Data jobs in Nebraska are:

What job categories do people searching Clinical Data Associate jobs in Nebraska look for?

The top searched job categories for Clinical Data Associate jobs in Nebraska are:

What cities in Nebraska are hiring for Clinical Data Associate jobs?

Cities in Nebraska with the most Clinical Data Associate job openings:

Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Nebraska as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $77,249 per year, or $37.1 per hour.

Clinical Research Data Sr Associate

Nebraska Medicine

Omaha, NE • On-site

Full-time

Posted 3 days ago

New

Nebraska Medicine rating

7.5

Company rating: 7.5 out of 10

Based on 155 frontline employees who took The Breakroom Quiz

231st of 898 rated healthcare providers

Job description

Serious Medicine is what we do. Being extraordinary is who we are. Every colleague plays a key role in upholding this promise to our patients and their families.
Shift:
First Shift (United States of America)
Shift Details:
M-F 8am - 5pm
Hybrid - this position does have in office requirements.
Why Work at Nebraska Medicine?
  • Together. Extraordinary. Join a team that values your skills, delivering exceptional care through collaboration.
  • Leading Health Network Work with the region's top academic health network, partnering with UNMC to transform lives through education, research, and patient care.
  • Dignity and Respect: We value all backgrounds and experiences, reflecting the communities we serve.
  • Educational Support Enjoy up to $5,000/year in tuition assistance, a 35% discount at Clarkson College, and career advancement opportunities with covered educational costs. Enjoy support for your personal growth within the organization, from those just starting their healthcare careers to those who are years down the path.

Be part of something extraordinary at Nebraska Medicine!
Responsible for the collection and review of clinical protocol research and registry data. Interpret data (including appropriate source documentation) for entry into computerized databases. Creates tools related to data collection for clinical research conducted by investigators. Provide support to Blood and Marrow Transplant and Cellular Therapy program through data collection, research protocol management, and other clinical research duties. Manage stem cell donor search requests. Maintain and communicate donor search progress to the clinical team. Negotiate and coordinate procurement of donor stem cell products in accordance with the patient's transplant timeline. Coordinate internal unrelated donor collections with clinical team, serving as a liaison between donor, Donor Center and the NMDP.
Required Qualifications:
• Minimum of one year data collection or data management experience required.
• High school education or equivalent required.
• Bachelor's degree in health science or related field or equivalent combination of education/experience combined (One year of experience equals one year of education) required.
• Proficient in Microsoft Office including Excel and Word required.
• Excellent organizational skills required. Ability to prioritize multiple tasks/responsibilities required.
• Knowledge of clinical research and records review required.
• Good verbal and written communication skills required.
• Computer literacy required. Ability to work effectively with other team members required.
• Strong interpersonal skills required.
Preferred Qualifications:
• Oncology/hematology experience preferred.
• Experience and/or knowledge of clinical trials and registry preferred.
• Prior experience working with physicians preferred.
• Bachelor's degree in health science or related field preferred.
• Experience with web based data entry systems (MediData, RAVE) preferred.
• Knowledge of medical terminology preferred. Database system knowledge preferred.
• Experience with Microsoft Access, PowerPoint, and Outlook preferred.
• Knowledge of Epic EMR preferred.
Nebraska Medicine is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, marital status, sex, age, national origin, disability, genetic information, sexual orientation, gender identity and protected veterans' status.

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