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Clinical Data Analyst Jobs in Reno, NV (NOW HIRING)

This position will serve as the primary clinical contact for external users for designated product ... Perform analysis of workflows, data collection, report details, and other technical issues ...

This position will serve as the primary clinical contact for external users for designated product ... Perform analysis of workflows, data collection, report details, and other technical issues ...

Principal Trainer-Clinical

Reno, NV · On-site

$37.92 - $53.10/hr

This position will serve as the primary clinical contact for external users for designated product ... Perform analysis of workflows, data collection, report details, and other technical issues ...

Clinical Pharmacist-Outpatient I

Reno, NV · On-site

$58.76 - $77.56/hr

... analysis of drug utilization data to identify trends, develop strategies and make recommendations for implementing comprehensive programs to improve patient outcomes. Provides committee support as ...

Clinical Pharmacist-Outpatient I

Reno, NV

$118K - $141K/yr

... analysis of drug utilization data to identify trends, develop strategies and make recommendations for implementing comprehensive programs to improve patient outcomes. Provides committee support as ...

Clinical Pharmacist-Outpatient I

Reno, NV

$118K - $141K/yr

... analysis of drug utilization data to identify trends, develop strategies and make recommendations for implementing comprehensive programs to improve patient outcomes. Provides committee support as ...

Position Purpose The Clinical Coordinator-RN is a registered nurse who has expertise in fields such ... data collection, feedback, and analysis. • Develops quality filters, audits, and case reviews ...

Clinical Coordinator-RN

Reno, NV · On-site

$34.40 - $48.16/hr

Position Purpose The Clinical Coordinator-RN is a registered nurse who has expertise in fields such ... data collection, feedback, and analysis. • Develops quality filters, audits, and case reviews ...

Position Purpose The Clinical Coordinator-RN is a registered nurse who has expertise in fields such ... data collection, feedback, and analysis. • Develops quality filters, audits, and case reviews ...

Clinical Coordinator-RN Cardiology

Reno, NV · On-site

$34.40 - $48.16/hr

Position Purpose The Clinical Coordinator-RN is a registered nurse who has expertise in fields such ... data collection, feedback, and analysis. • Develops quality filters, audits, and case reviews ...

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Clinical Data Analyst information

See Reno, NV salary details

$17

$36

$60

How much do clinical data analyst jobs pay per hour?

As of Aug 1, 2026, the average hourly pay for clinical data analyst in Reno, NV is $36.25, according to ZipRecruiter salary data. Most workers in this role earn between $29.23 and $41.92 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Data Analyst, you need a solid background in data analysis, statistics, and healthcare concepts, often supported by a degree in health informatics, statistics, or a related field. Familiarity with data management tools, programming languages like SQL or Python, and statistical software such as SAS or R, as well as knowledge of clinical databases and regulations like HIPAA, is crucial. Strong attention to detail, problem-solving abilities, and effective communication skills help you interpret complex data and convey insights to multidisciplinary teams. These skills ensure accurate data analysis, support evidence-based decision-making, and maintain compliance within clinical research and healthcare environments.

What are some common challenges Clinical Data Analysts face when ensuring data quality and integrity?

Clinical Data Analysts frequently encounter challenges such as inconsistent data entry, missing values, and discrepancies across various data sources. Ensuring data quality requires meticulous attention to detail and strong communication with clinical staff to resolve ambiguities or errors. Analysts also navigate evolving regulatory requirements and must stay current with best practices in data validation and cleaning to maintain compliance and reliability of clinical trial results. Collaborating closely with data managers, statisticians, and clinical teams is essential for addressing these challenges efficiently.

What is a Clinical Data Analyst?

A Clinical Data Analyst is a professional who manages and analyzes healthcare data to support clinical research and improve patient outcomes. They collect, process, and ensure the accuracy of medical data from clinical trials or healthcare systems. Their work helps identify trends, support decision-making, and ensure compliance with regulatory standards. Clinical Data Analysts often use specialized software to clean, validate, and report on large datasets. They play a critical role in maintaining the integrity and quality of clinical information.

Is 40 too late for data science?

For a Clinical Data Analyst or similar data science roles, starting at age 40 is not too late. Many professionals successfully transition into data science later in their careers by acquiring relevant skills such as programming, statistics, and data management, often through online courses or certifications. Experience in healthcare or clinical environments can also be valuable in this field.

Do you need a degree to be a healthcare data analyst?

A degree is often preferred for a clinical data analyst role, but relevant experience, technical skills in data management and analysis, and proficiency with tools like SQL and Excel can also qualify candidates. Some employers may accept certifications or specialized training in healthcare data or informatics instead of a formal degree.

What healthcare jobs pay over $100k per year?

Clinical Data Analysts can earn over $100,000 annually, especially with experience, advanced skills in data management and statistical software, and certifications like Certified Health Data Analyst (CHDA). Other high-paying healthcare roles include physicians, surgeons, healthcare executives, and specialized nurses, often requiring advanced degrees and extensive experience.
What are the most commonly searched types of Clinical Data Analyst jobs in Reno, NV? The most popular types of Clinical Data Analyst jobs in Reno, NV are:
What are popular job titles related to Clinical Data Analyst jobs in Reno, NV? For Clinical Data Analyst jobs in Reno, NV, the most frequently searched job titles are:
What job categories do people searching Clinical Data Analyst jobs in Reno, NV look for? The top searched job categories for Clinical Data Analyst jobs in Reno, NV are:
Infographic showing various Clinical Data Analyst job openings in Reno, NV as of July 2026, with employment types broken down into 78% Full Time, 20% Part Time, 1% Contract, and 1% Nights. Highlights an 90% In-person, and 10% Remote job distribution, with an average salary of $75,403 per year, or $36.3 per hour.

$22/hr

Other

Medical, Retirement, PTO

Re-posted 13 days ago


Charles River Laboratories rating

8.3

Company rating: 8.3 out of 10

Based on 93 frontline employees who took The Breakroom Quiz

20th of 86 rated pharmaceutical


Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.

Job Overview

We are seeking a Data Review Analyst I at our Safety Assessment site located in Reno, NV.

Basic Summary:

Provides administrative, logistical and technical support for Scientific staff conducting studies or supporting functions for operations of the laboratory. Coordinates all laboratory support, pre-study activities, method development, method validation, study activities, data and/or reporting activities. Responsible for data review for completeness, quality or QC against the applicable protocol or procedure. May be responsible for drafting client correspondence, study correspondence, reporting or direct client interaction. Interacts with other departments, scientific staff, and sponsors either locally or across sites.

 

Job Description

The Data Review Analyst I is responsible for QC reviewing all tabulated study data to ensure it is accurate and complete. Ensure that all data received for review follows SOP guidelines that apply to the recording of study data.
Complete QC for tabulated study data produced in operational departments.
    Ensure all report table corrections are completed by the appropriate staff members and that they are completed correctly.
    Demonstrate comprehension of applicable regulatory driving documents, including protocols/phase plans, Analytical Procedures, Data Transfer Agreements, SOPs/BOPs, etc. as they relate to reported study data.
    Ensure sample analysis data collected is appropriate and in scope with driving documents (protocol/phase plans, Analytical Procedures, Data Transfer Agreements, SOPs/BOPs, etc.) for what is intended to be reported.
    Develop effective communication skills through informal discussions with peers, supervisor, and team.
    Develop critical thinking, troubleshooting, and time management skills to ensure data quality and study timelines are maintained.
    Identify process improvement initiatives based on observed trends and errors.
    Support data review assistants with data review on all paper and electronic data produced in operational departments as needed.
    Support with archiving, collating, and organizing all completed and reviewed data and/or file as needed.
    Perform all other related duties as assigned.

The following are minimum qualifications related to the Data Review Analyst I position:


    Education: High school diploma or General Education Degree (G.E.D.) required. 
    Experience: Minimum of 2-4 years related experience, including GLP and/or GCP experience required, or must have demonstrated full knowledge of competencies and positive performance at the previous level.
    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
    Certification/Licensure: None
    Other: Strong organizational skills and acute attention to detail. Proficient in utilizing personal computer, e-mail, and standard office software packages (word processing, spreadsheet, presentation, database). Basic understanding of processes used for study data collection. Basic understanding of SOPs, GLPs, and other applicable regulatory guidelines governing the recording and review of study data.
 

The pay range for this position is $22.00 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.  Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.


About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We're committed to providing benefits that elevate your quality of life.  Based on your position these may include:  bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.


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About Charles River

Sourced by ZipRecruiter

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947