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

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 ...

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 · 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 ...

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

$66.01 - $87.13/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 ...

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 ...

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 ...

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 ...

Clinical Coordinator-RN - Neurology

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 ...

This position will serve as the primary clinical contact for external users for designated product ... Managers, vendors, and customers. • Perform analysis of workflows, data collection, report ...

This position will serve as the primary clinical contact for external users for designated product ... Managers, vendors, and customers. • Perform analysis of workflows, data collection, report ...

Showing results 21-40

Clinical Data Management information

See Reno, NV salary details

$19

$57

$81

How much do clinical data management jobs pay per hour?

As of Aug 21, 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 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 the key skills and qualifications needed to thrive in clinical data management?

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.

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.

How do I become a clinical data management?

To become a clinical data manager, typically a bachelor's degree in life sciences, healthcare, or related fields is required. Gaining experience with clinical trial processes, data management tools like EDC systems, and obtaining certifications such as the Society for Clinical Data Management (SCDM) certification can enhance job prospects.

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 August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $118,560 per year, or $57 per hour.

Clinical Lab Scientist - Per Diem

Tahoe Forest Health

Truckee, CA • On-site

$68.07/hr

Part-time

Posted 29 days ago


Job description

Bargaining Unit: EAP

Rate of Pay: $68.07/hour + DOE + Shift Differential (Base Pay of $60.51 includes 12.5% per diem premium)

Summary
Under the direction of Clinical Laboratory management staff and in accordance with regulatory requirements and accreditation standards; performs clinical laboratory functions in a timely manner following specified policies, procedures and protocols. On a 24x7 basis performs analysis on blood, body fluids, tissues and other material from patients/clients to provide data for diagnosis, treatment, and prevention of disease.

Essential Duties and Responsibilities

  • As defined by delegation from the medical director for the duties of the “general supervisor” and in accordance with CLIA-88, State of California and the State of Nevada regulations performs the following:
  • Consistently complies with all applicable Tahoe Forest Health System and Clinical Laboratory policies and procedures. Evaluates and solves problems or notifies management of all unresolved operational problems.
  • Performs complex analytical tests and procedures, recognizes deviation from expected results, and takes appropriate action to maintain accuracy and precision. Ensures data is entered into the LIS (laboratory information system) in a timely manner.
  • Effectively communicates with nursing, physicians and other ancillary staff to ensure effective patient preparation, collection and specimen handling. Significant errors or deviation from established Standard Operating Procedures (SOPs) are reported within the Clinical Laboratory through the Continuous Service Improvement (CSI) process or through the Tahoe Forest Health System “RLDatix” risk management system
  • Recognizes factors that affect measurements and results, analyzes Quality Control (QC) data, makes judgments concerning the results, and takes appropriate action to maintain accuracy and precision.
  • Recognizes abnormal test results and answers inquiries about them, the methodology, specificity, and sensitivity; answers questions about specific factors that can influence test results.
  • Operates and maintains instrument/equipment, recognizes equipment malfunction, troubleshoots and repairs as necessary. Notifies clinical departments in a timely manner when equipment/instruments are down and testing may be delayed. Takes appropriate actions to activate backup activities when appropriate to ensure safe patient care.
  • When confronted with operational issues, acts as the “Medicare Supervisor”/ ”General Supervisor” per CLIA-88 regulations in the absence of laboratory management staff. “TFHS CLS/”Medicare Supervisor” Responsibilities available in department.
  • Maintains current knowledge related to patient safety and laboratory safety requirements. Observes and ensures the health and safety requirements for patients and employees both within and outside of the clinical laboratory environment are achieved.
  • Consistently contributes to process improvement activities within and outside of the Clinical Laboratory using “lean principles” and Define-Measure-Analyze-Improve Control (DMAIC) approach to enhance operations. Helps evaluate new techniques and procedures in terms of space and personnel requirements, method comparison, cost analysis, and the establishment of reference intervals; writes, revises and/or reviews technical procedures.
  • Some support tasks will be required at times to ensure effective laboratory operations including but not limited to telephone attendance, clerical duties, inventory management, customer service activities, specimen collection, sample handling and special procedures. Training and mentoring new personnel may be assigned.
  • Scheduling of hours may be changed as necessary to meet the needs of laboratory operations. The ability to work standby and take call back is required to cover situations when no staff is routinely scheduled or schedule is vacant.
  • Demonstrates System Values in performance and behavior. Understands “Just Culture” utilization at TFHS.
  • Complies with System policies and procedures.
  • Other duties as may be assigned.

Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Supervisory Responsibilities
No supervisory responsibilities.

Minimum Education/Experience
Bachelor's Degree or higher in a health science related discipline or has fulfilled military requirements to acquire a CA CLS license.

1-2 years relevant experience

Required Licenses/Certifications
California Clinical Laboratory Scientist (CLS)

  • Upon hire

OR

Nevada Clinical Laboratory Technologist-General Supervisor License

  • Upon hire

Other Experience/Qualifications
Required:

  • California Clinical Laboratory Scientist and/or Nevada Clinical Laboratory Technologist- General Supervisor license.
  • Required license based on worksite state
  • Functionally knowledgeable of the principles, practices and procedures in a hospital based clinical laboratory environment.

Preferred:

  • Concurrent dual licensure in California and Nevada.
  • Operations experience in the areas of chemistry, hematology, serology, coagulation, transfusion, parasitology and microbiology.
  • Three (3) years of experience as a Clinical Laboratory Scientist.
  • Previous experience in a hospital laboratory setting.
  • Microbiology, Phlebotomy and EKG experience.