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

... management process other than: • Performance of review of service request for completeness of information • Collection and transfer of non-clinical data. Such data may include demographic ...

... management process other than: • Performance of review of service request for completeness of information • Collection and transfer of non-clinical data. Such data may include demographic ...

Referral Specialist

Reno, NV · On-site

$17.37 - $24.32/hr

... management process other than: • Performance of review of service request for completeness of information • Collection and transfer of non-clinical data. Such data may include demographic ...

Clinical Coordinator-RN

Reno, NV · On-site

$34.40 - $48.16/hr

... of data. • Supports planning and participates in clinical research as approved or directed. • Evaluates and reports to departmental/organizational senior management on status and changes in ...

Clinical Pharmacist-Outpatient I

Reno, NV · On-site

$58.76 - $77.56/hr

Provides committee support as needed for formulary management across the continuum of care. In ... data to identify trends, and recommend strategies for reducing the overall drug spend across the ...

... of data. • Supports planning and participates in clinical research as approved or directed. • Evaluates and reports to departmental/organizational senior management on status and changes in ...

... of data. • Supports planning and participates in clinical research as approved or directed. • Evaluates and reports to departmental/organizational senior management on status and changes in ...

Clinical Pharmacist-Outpatient I

Reno, NV · On-site

$118K - $141K/yr

Provides committee support as needed for formulary management across the continuum of care. In ... data to identify trends, and recommend strategies for reducing the overall drug spend across the ...

Clinical Pharmacist-Outpatient I

Reno, NV · On-site

$118K - $141K/yr

Provides committee support as needed for formulary management across the continuum of care. In ... data to identify trends, and recommend strategies for reducing the overall drug spend across the ...

Reno Orthopedic Center wants you to join the team as a Clinical Manager! We are seeking an ... You will oversee daily operations, analyze performance data, implement process improvements ...

Reno Orthopedic Center wants you to join the team as a Clinical Manager! We are seeking an ... You will oversee daily operations, analyze performance data, implement process improvements ...

Clinical Pharmacist-Outpatient I

Reno, NV

$118K - $141K/yr

Provides committee support as needed for formulary management across the continuum of care. In ... data to identify trends, and recommend strategies for reducing the overall drug spend across the ...

Reno Orthopedic Center wants you to join the team as a Clinical Manager! We are seeking an ... You will oversee daily operations, analyze performance data, implement process improvements ...

Clinical Coordinator-RN Cardiology

Reno, NV · On-site

$34.40 - $48.16/hr

... of data. • Supports planning and participates in clinical research as approved or directed. • Evaluates and reports to departmental/organizational senior management on status and changes in ...

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Clinical Data Management information

See Reno, NV salary details

$19

$57

$81

How much do clinical data management jobs pay per hour?

As of Jul 20, 2026, the average hourly pay for clinical data management in Reno, NV is $57.00, according to ZipRecruiter salary data. Most workers in this role earn between $45.05 and $67.84 per hour, depending on experience, location, and employer.

What is the work of clinical data management?

Clinical data management involves collecting, cleaning, and maintaining data generated during clinical trials to ensure accuracy, completeness, and consistency. It includes designing data collection tools, validating data, and managing databases using specialized software, often requiring attention to regulatory standards and good clinical practice. The role is essential for supporting reliable analysis and decision-making in drug development.

What is clinical data management?

Clinical data management (CDM) is a critical process in clinical research that involves collecting, cleaning, and managing data generated during clinical trials. The goal is to ensure that the data is accurate, reliable, and compliant with regulatory standards. CDM professionals work closely with researchers, statisticians, and regulatory bodies to validate data and ensure its integrity throughout the study. This process helps in making informed decisions about the safety and efficacy of new drugs or treatments.

What are some common challenges faced by professionals in Clinical Data Management, and how can they be addressed?

One of the common challenges in Clinical Data Management is ensuring data accuracy and consistency across multiple sources and formats. This often involves resolving discrepancies and managing large volumes of data within tight timelines. Effective communication with clinical research associates, statisticians, and IT teams is crucial to address data queries promptly and maintain data integrity. Staying updated with regulatory requirements and leveraging advanced data management systems can also help mitigate these challenges and improve overall workflow efficiency.

What is the difference between Clinical Data Management vs Clinical Data Coordinator?

AspectClinical Data ManagementClinical Data Coordinator
ResponsibilitiesDesigning data collection processes, database setup, data validation, and ensuring data quality for clinical trials.Collecting, reviewing, and entering clinical trial data, ensuring accuracy and completeness.
Required SkillsKnowledge of data management systems, clinical trial processes, and data validation techniques.Attention to detail, data entry skills, familiarity with clinical trial documentation.
Work EnvironmentTypically in clinical research organizations, pharmaceutical companies, or CROs.Often within clinical sites or research teams supporting data collection activities.

While both roles focus on clinical trial data, Clinical Data Management involves designing and overseeing data systems and ensuring data integrity, whereas Clinical Data Coordinators handle the day-to-day data collection and entry tasks. Both are essential for successful clinical research but differ in scope and responsibilities.

Is clinical data management a good career?

Clinical data management is a vital role in the healthcare and pharmaceutical industries, involving the collection, validation, and analysis of clinical trial data. It requires knowledge of data management tools, regulatory standards, and attention to detail, offering opportunities for career growth and specialization. The field is generally considered stable with increasing demand due to ongoing clinical research activities.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical trials, monitoring, or related roles. Entry-level roles in clinical data management or clinical research may include assistant or coordinator positions, with CRAs often needing a background in life sciences, healthcare, or related certifications. Advancement to CRA roles generally involves gaining experience and developing skills in regulatory compliance and trial monitoring tools.

What are the key skills and qualifications needed to thrive in Clinical Data Management, and why are they important?

To thrive in Clinical Data Management, you need a strong background in life sciences, attention to detail, and understanding of clinical trial processes, often supported by a relevant degree. Familiarity with industry-standard data management systems such as Medidata Rave or Oracle Clinical, as well as knowledge of CDISC standards and regulatory requirements, is essential. Excellent organizational skills, communication, and problem-solving abilities help ensure data integrity and effective cross-functional collaboration. These skills and qualities are crucial for ensuring high-quality, compliant data that supports clinical research and regulatory submissions.

How do I become a Clinical Data Manager?

To become a Clinical Data Manager, typically a bachelor's degree in life sciences, healthcare, or a related field is required. Relevant skills include knowledge of clinical trial processes, data management tools like EDC systems, and attention to detail; certifications such as CDMP can enhance job prospects. Gaining experience through internships or entry-level roles in clinical research is also beneficial.
What are popular job titles related to Clinical Data Management jobs in Reno, NV? For Clinical Data Management jobs in Reno, NV, the most frequently searched job titles are:
What job categories do people searching Clinical Data Management jobs in Reno, NV look for? The top searched job categories for Clinical Data Management jobs in Reno, NV are:
What cities near Reno, NV are hiring for Clinical Data Management jobs? Cities near Reno, NV with the most Clinical Data Management job openings:
Infographic showing various Clinical Data Management job openings in Reno, NV as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $118,560 per year, or $57 per hour.
2025 Fall Intern, Clinical Applications

2025 Fall Intern, Clinical Applications

Zimmer Biomet

Carson City, NV • On-site

$14.75 - $19.50/hr

Other

Re-posted 29 days ago


Zimmer Biomet rating

7.7

Company rating: 7.7 out of 10

Based on 96 frontline employees who took The Breakroom Quiz

198th of 430 rated machine equipment manufacturers


Job description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.  

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards.  We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of software used in clinical research, primarily the Clinical Trial Management System (CTMS). 

How You'll Create Impact
  • Assist in testing and maintaining clinical software applications under the guidance of experienced developers and analysts.
  • Support the documentation of technical processes, user guides, and validation protocols.
  • Participate in requirements gathering sessions with stakeholders to better understand business and user needs.
  • Help monitor and track system issues, assisting in troubleshooting with supervision.
  • Perform basic data checks and assist with data validation efforts to ensure data integrity.
  • Observe and support user training sessions and help prepare training materials as needed.
What Makes You Stand Out
  • Strong written and verbal communication skills.
  • Ability to manage time effectively and handle multiple tasks or assignments under supervision.
  • Ability to work collaboratively as part of a team and communicate effectively with both technical and non-technical stakeholders.
  • Detail-oriented mindset with the ability to follow documented procedures and best practices.
  • Curiosity and willingness to learn about clinical applications and how technology supports clinical trials and research.
  • Proficiency in Microsoft Office tools, especially Excel, Word, and PowerPoint.
  • Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or similar.
  • Basic understanding of relational databases and familiarity with writing or reading simple SQL queries is a plus.
  • Interest in web development and knowledge of HTML and CSS, or UX/UI is a plus.
Your Background
  • Must be actively enrolled in an academic program for the entire duration of the assignment
  • Must be available to work full-time (40 hours/week) throughout the co-op session
  • Must be authorized to work in the U.S. without requiring employer sponsorship
  • Pursuing a bachelor’s degree in Computer Science, Information Systems, Health Informatics, Data Science, or related field.
  • A minimum GPA of 3.0 is strongly preferred
Travel Expectations
  • Up to 5%

EOE/M/F/Vet/Disability


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About Zimmer Biomet

Sourced by ZipRecruiter

Zimmer Biomet is a global medical technology leader. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Warsaw, IN, US

Year founded

1927

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