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Statistics Validator Jobs in Decatur, GA (NOW HIRING)

In this vital role you will provide both strategic oversight and hands-on statistical programming ... validating SDTM, ADaM datasets, and TFLs Thorough understanding of clinical trial processes from ...

Partner with operations analysts to design robust experimental frameworks, including success criteria, measurement methodologies, and statistical validation approaches. * Analyze complex, multi ...

Perform statistical analysis and hypothesis testing to identify patterns and trends * Apply machine learning techniques for predictive modeling and forecasting * Validate models and ensure analytical ...

... • Validate data accuracy and resolve data quality issues across multiple financial and ... Required : • Bachelor's degree in a quantitative field such as statistics, computer science ...

Job Title This position is responsible for developing, implementing, and validating utilization and ... Reviews and prepares reports, compiles statistics, and analyzes data regarding dentists that are ...

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Statistics Validator information

See Decatur, GA salary details

$39.5K

$81.7K

$114.2K

How much do statistics validator jobs pay per year?

As of Jun 28, 2026, the average yearly pay for statistics validator in Decatur, GA is $81,677.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,600.00 and $113,300.00 per year, depending on experience, location, and employer.

What are Statistics Validators?

Statistics Validators are professionals who verify the accuracy, integrity, and reliability of statistical data and analyses. They review datasets, methodologies, and statistical outputs to ensure that findings are valid and meet relevant standards. Their work is crucial in research, government, and industry settings, where credible data is essential for decision making. By checking for errors, inconsistencies, and biases, Statistics Validators help maintain the quality and trustworthiness of statistical information.

What are the primary challenges a Statistics Validator faces when ensuring data integrity within a project?

Statistics Validators often encounter challenges related to data quality, such as incomplete datasets, inconsistent formats, or errors introduced during data collection and entry. They must meticulously review data sources, cross-check results, and ensure that statistical methodologies are correctly applied. Collaboration with data analysts, researchers, and IT teams is essential to resolve discrepancies and maintain high data standards. Staying up-to-date with industry best practices and regulatory requirements also plays a crucial role in overcoming these challenges.

What is the difference between Statistics Validator vs Data Analyst?

AspectStatistics Validator
Required CredentialsTypically a degree in statistics, mathematics, or related field; certifications like CAP or ASA are common
Work EnvironmentPrimarily office-based, working with data validation processes, quality assurance, and compliance
Employer & IndustryFinancial institutions, research organizations, government agencies, and data-driven companies
Comparison with Data Analyst

The main difference between a Statistics Validator and a Data Analyst lies in their focus. A Statistics Validator specializes in verifying the accuracy and integrity of statistical data, ensuring compliance with standards. In contrast, a Data Analyst interprets data to generate insights and support decision-making. While both roles require strong statistical knowledge, the validator emphasizes quality assurance, whereas the analyst emphasizes data interpretation and reporting.

What are the key skills and qualifications needed to thrive as a Statistics Validator, and why are they important?

To thrive as a Statistics Validator, you need a strong background in statistics, data analysis, and quality assurance, often supported by a degree in statistics, mathematics, or a related field. Familiarity with statistical software such as R, SAS, or SPSS, as well as proficiency in data validation frameworks and reporting tools, is typically required. Attention to detail, critical thinking, and strong communication skills help ensure the accuracy and clarity of validated data. These skills and qualities are crucial for maintaining data integrity, supporting decision-making, and upholding the credibility of statistical results.
What job categories do people searching Statistics Validator jobs in Decatur, GA look for? The top searched job categories for Statistics Validator jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Statistics Validator jobs? Cities near Decatur, GA with the most Statistics Validator job openings:

Biostatistical Prograrmming Manager

Amgen

Atlanta, GA • On-site

Full-time

This job post has expired today. Applications are no longer accepted.


Key responsibilities

  • Provide rapid response statistical programming support for urgent internal and external requests.

  • Serve as a lead programmer for studies and projects, including Data Access Plan activities, unblinding efforts, and special projects.

  • Oversee the execution and quality of projects managed by FSP partners according to the Global Statistical Programming Quality Oversight Plan.


Job description

Career CategoryClinicalJob Description

Biostatistical Programming Manager

What you will do

Let's do this. Let's change the world. In this vital role you will provide both strategic oversight and hands-on statistical programming support to enable high-quality and timely clinical trial deliverables.

This role is part of the centrally managed Quality and Quick Response (QQR) Programming team and is responsible for supporting urgent and high-priority programming needs across development programs. The manager will serve as a technical programming expert who can rapidly respond to internal and external requests, support special projects, provide global quality oversight, and contribute directly to programming deliverables when needed.

This role will primarily support programs within the Obesity Therapeutic Area and requires close collaboration with cross-functional teams to support fast-paced development activities and evolving business priorities.

Responsibilities

Provide rapid response statistical programming support for urgent internal and external requests

Serve as a lead programmer for studies and projects, such as Data Access Plan (DAP) activities, unblinding efforts, and special projects

Deliver hands-on programming support for SDTM, ADaM, Tables, Listings, and Figures (TFLs), and other study and regulatory submission deliverables as needed

Oversee the execution and quality of projects managed by our FSP partners per Amgen Global Statistical Programming (GSP) Quality Oversight Plan (QOP)

Ensure that FSP and in-house programming deliverables meet quality, compliance, timeline, and productivity expectations

Mitigate at-risk projects by providing technical expertise, programming support, and operational guidance

Contribute to training material development and delivery to internal teams and FSP partners

Provide guidance and technical consultancy to study programming team on Amgen processes, tools, and utilities

Lead/contribute to GSP continuous improvement iniatives and support cross-functional initiatives including inspection readiness, process improvement, innovation, and training activities

Contribute to programming team performance metrics development, data collection, and reporting

Review project documentation such as specifications, issue logs, deliverable status for accuracy and completeness

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a manager with these qualifications.

Basic Qualifications:

Doctorate degree OR

Master's degree and 2 years of statistical programming experience OR

Bachelor's degree and 4 years of statistical programming experience OR

Associate's degree and 8 years of statistical programming experience OR

High school diploma / GED and 10 years of statistical programming experience

Preferred Qualifications:

Masters in Computer Science, Statistics, Mathematics, Computer Science, Life Sciences or another relevant scientific subject

6+ years of statistical programming in biopharmaceutical industry

Regulatory submission experience

Strong hands-on SAS programming expertise including SAS Base, Macro, SQL, SAS/Graph and Stat packages

Experience with R programming for clinical trial analyses, data manipulation, reporting and visualization preferred

Familiarity with additional programming languages and tools such as Python preferred

Hands-on experience developing and validating SDTM, ADaM datasets, and TFLs

Thorough understanding of clinical trial processes from data collection through analysis and reporting

Ability to lead programmers in successful completion of all study programming activities and provide guidance on technical and process questions

Strong understanding of data standards and compliance checks including Pinnacle 21

Experience providing quality oversight for outsourced and internal programming deliverables

Ability to troubleshoot complex technical issues and turnaround at-risk projects

Experience working in a globally dispersed team on Phase 1-4 clinical trials

Experience supporting clinical development programs within the Obesity Therapeutic Area preferred

Understanding of obesity clinical endpoints, data standards, and regulatory considerations is highly desirable

Excellent oral and written English communication skills; strong collaboration, negotiation, and organizational skills

.

Salary Range

129,056.35USD -174,605.65USD