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Clinical Data Associate Jobs in Nevada (NOW HIRING)

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Collect, record, and maintain accurate clinical research data and source documentation in ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Collect, record, and maintain accurate clinical research data and source documentation in ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Collect, record, and maintain accurate clinical research data and source documentation in ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

UNLV Health

Authorization Specialist - Per Diem

Las Vegas, NV · On-site

$17.25 - $23/hr

Coordinate rapidly with ordering practitioners to supply missing clinical data or schedule payer-to ... Associate degree or healthcare administration coursework preferred. Qualifications * Two years of ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$30/hr

Collect, record, and maintain accurate clinical research data and source documentation in ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

Danaher

Principal Clinical Scientist

Las Vegas, NV · On-site +1

Our associates are involved in every stage of diagnostics, from ideation to development and ... Ability to critically review and interpret scientific and clinical trial data, and oversee the ...

PRISM Vision Group

PET-CT Tech

Las Vegas, NV · On-site

Assists with the collection of clinical data for patient follow-up and development of teaching and ... Associates or Bachelors degree in Nuclear Medicine Technology or from an AMA accredited program or ...

The US Oncology Network

PET-CT Tech

Las Vegas, NV · On-site

Assists with the collection of clinical data for patient follow-up and development of teaching and ... Associates or Bachelors degree in Nuclear Medicine Technology or from an AMA accredited program or ...

The US Oncology Network

PET-CT Tech

Las Vegas, NV · On-site

Assists with the collection of clinical data for patient follow-up and development of teaching and ... Associates or Bachelors degree in Nuclear Medicine Technology or from an AMA accredited program or ...

PRISM Vision Group

PET-CT Tech

Henderson, NV · On-site

Assists with the collection of clinical data for patient follow-up and development of teaching and ... Associates or Bachelors degree in Nuclear Medicine Technology or from an AMA accredited program or ...

The US Oncology Network

PET-CT Tech

Henderson, NV · On-site

Assists with the collection of clinical data for patient follow-up and development of teaching and ... Associates or Bachelors degree in Nuclear Medicine Technology or from an AMA accredited program or ...

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Nevada

Clinical Data Associate information

See Nevada salary details

$14

$39

$88

How much do clinical data associate jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for clinical data associate in Nevada is $39.66, according to ZipRecruiter salary data. Most workers in this role earn between $29.86 and $39.66 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 Nevada?

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

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

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

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

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

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

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

Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Nevada as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 9% Part Time, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $82,503 per year, or $39.7 per hour.

Clinical Research Coordinator

Las Vegas, NV • On-site

System One
Business Consulting Services • 5 - 10K employees
Learn more about System Oneexternal

$23.25 - $30.75/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 18 days ago

Job description

Job Title: Clinical Research Coordinator Location: Las Vegas, NV Onsite Hours/Schedule: 40 hours Type: Contract Responsibilities

  • Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff.
  • Conduct screening visits to collect medical history & other information from study participants.
  • Assist with informed consent and enrollment of study participants in accordance with protocol requirements and ethical guidelines.
  • Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams.
  • Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards.
  • Communicate with study participants to provide education, answer questions, and support adherence to study requirements.
  • Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team.
  • Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines.
  • Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in accordance with regulations (if qualified.)
  • Scan, upload, file, and maintain organized study records and documentation.
  • Apply critical thinking skills to support efficient study operations and problem resolution.
  • Perform other duties as assigned.

Requirements

  • High school diploma or equivalent required; an associate’s degree or higher in a health-related field preferred.
  • Basic knowledge of clinical research strongly preferred.
  • Medical terminology & patient care experience required.
  • Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities.
  • Ability to communicate clearly and professionally with diverse populations.
  • Ability to work collaboratively in a fast-paced, team-oriented environment.
  • Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines strongly preferred.
  • Experience with participant screening and the informed consent process strongly preferred.
  • Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred.
  • Medical Assistant (MA) certification preferred, Current CPR/BLS certification preferred, Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #LI-AD3 Ref: #568-Clinical

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About System One

Sourced by ZipRecruiter

System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.

Industry

Business consulting services and recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Pittsburgh, PA, US

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