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Clinical Data Associate Jobs in Nebraska (NOW HIRING)

Participate in quality improvement, data tracking, budgeting activities, marketing initiatives, and ... Associate benefits are designed to encourage personal wellness and smart healthcare decisions for ...

Supports metric / KPI programs, with timely and complete data documentation, reporting, and ongoing ... Associate or Bachelor's degree from an accredited School of Nursing. * Advanced degree BSN or MSN ...

Clinical Educator

Omaha, NE · On-site

$85K - $157K/yr

Associate/Bachelors/BSN or equivalent work-related experience * 2 years' experience working in ... with data, science, and technology to deliver bespoke engagement solutions that help clients ...

Clinical Educator

Omaha, NE · On-site

$85K - $157K/yr

Associate/Bachelors/BSN or equivalent work-related experience * 2 years' experience working in ... with data, science, and technology to deliver bespoke engagement solutions that help clients ...

Clinical Educator

Omaha, NE · On-site

$85K - $157K/yr

Associate/Bachelors/BSN or equivalent work-related experience * 2 years' experience working in ... with data, science, and technology to deliver bespoke engagement solutions that help clients ...

Associate/Bachelors/BSN or equivalent work-related experience * 2 years' experience working in ... with data, science, and technology to deliver bespoke engagement solutions that help clients ...

Showing results 41-60

Clinical Data Associate information

See Nebraska salary details

$13

$37

$82

How much do clinical data associate jobs pay per hour?

As of Aug 16, 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 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 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 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 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 Nebraska?

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

What are popular job titles related to Clinical Data Associate jobs in Nebraska?

For Clinical Data Associate jobs in Nebraska, the most frequently searched job titles are:

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

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

Infographic showing various Clinical Data Associate job openings in Nebraska as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $77,249 per year, or $37.1 per hour.

Medical Laboratory Technician

Bryan Health

Lincoln, NE

Full-time

Re-posted 19 days ago


Bryan Health rating

7.1

Company rating: 7.1 out of 10

Based on 119 frontline employees who took The Breakroom Quiz

381st of 887 rated healthcare providers


Job description

GENERAL SUMMARY:

Performs high complexity medical laboratory tests, procedures, and analyses to provide data for diagnosis, treatment, and prevention of disease as part of the on the job clinical experience for the MLT or MLS career ladder.

PRINCIPAL JOB FUNCTIONS:

1. *Commits to the mission, vision, beliefs and consistently demonstrates our core values.

2. *Under the supervision of a Clinical Laboratory Improvement Amendment (CLIA)-designated General Supervisor (Medical Laboratory Scientist), performs laboratory testing according to laboratory standards, policies and procedures in a timely thorough manner.

3. *Assists with development and validation processes for MLT I competencies.

4. *Assists with clinical decision-making and interpretation of established procedures.

5. *Provides direction to MLT I and serves as clinical resource.

6. *Analyzes test results and enters data into the computer using laboratory standards, policies, and procedures.

7. *Performs and analyzes quality control measures to ensure accurate clinical data. Analyzes unacceptable quality control results and troubleshoots shifts or trends as necessary.

8. *Maintains competency and proficiency on all laboratory instrumentation and procedures; performs and documents preventive maintenance on laboratory instruments and equipment, troubleshooting problems as necessary. Notifies immediate supervisory personnel of equipment/instrument issues and calls Service regarding issues.

9. *Communicates with coworkers, clients and leadership by transmitting patient cart testing and results, appropriate ideas, information and opinions clearly, concisely and courteously; maintains employee, patient, client and corporate confidentiality.

10. *Performs general housekeeping tasks to maintain safe work environment; maintains adequate supplies in the work area.

11. *Assists in training new employees, students,other technical staff and support staff.

12. *Works collaboratively with all laboratory staff to ensure completion of testing and communication of necessary information to assist testing completion.

13. Uses quality improvement processes, programs or outcomes to help improve department operations; assists with LEAN projects.

14. Performs service excellence must-haves to achieve an excellent patient/customer experience.

15. Basic knowledge in phlebotomy and phlebotomy procedures and ability to perform phlebotomy if required by laboratory facility.

16. Maintains professional growth and development through seminars, workshops, and professional affiliations to keep abreast of latest trends in field of expertise.

17. Participates in meetings, committees and department projects as assigned.

18. Performs other related projects and duties as assigned.

(Essential Job functions are marked with an asterisk “*”. Refer to the Job Description Guide for the definition of essential and non-essential job functions.) Attach Addendum for positions with slightly different roles or work-specific differences as needed.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES:

1. Knowledge gained as a Specimen Processing Technician 2 of clinical laboratory equipment/instrumentation, test procedures and standards.

2. Knowledge of computer hardware equipment and software applications relevant to work functions.

3. Skill gained during on the job clinical training in the use and preventative maintenance of laboratory instruments and equipment.

4. Ability to work with mathematical concepts and apply such concepts to practical situations.

5. Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.

6. Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists and engage critical thinking skills.

7. Ability to communicate effectively both verbally and in writing.

8. Ability to perform crucial conversations with desired outcomes.

9. Ability to establish and maintain effective working relationships with all levels of personnel and medical staff.

10. Ability to work as a team member.

11. Ability to maintain confidentiality relevant to sensitive information.

12. Ability to prioritize work demands and work with minimal supervision.

13. Ability to maintain regular and punctual attendance.

EDUCATION AND EXPERIENCE:

Associate's degree in Medical Laboratory Technology or related laboratory science from a two-year accredited college or CLIA- approved Military MLT program required or has earned a Bachelor’s degree in a chemical, physical or biological science meeting American Society for Clinical Pathology (ASCP) criteria for MLT certification and with the 2 years of required clinical experience for ASCP certification. ASCP certification as an MLT (ASCP) or equivalency preferred.

PHYSICAL REQUIREMENTS:

(Physical Requirements are based on federal criteria and assigned by Human Resources upon review of the Principal Job Functions.)

(DOT) – Characterized as medium work requiring exertion of 20 to 50 pounds of force occasionally, and/or 10 to 25 pounds of force frequently, and/or a greater than negligible up to 10 pounds of force constantly to move objects.

*Must be able to distinguish and discriminate between colors.


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