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Associate Statistical Programmer Jobs in Grayson, GA

... associates and suppliers to perform effective problems solving using standard tools (8D, 3P and ... Work with customers and suppliers to refine their processes. · Excellent quantitative, statistical ...

Senior AI Engineer

Atlanta, GA · On-site

$156K - $234K/yr

This role requires associates to be in-office 1 - 2 days per week, fostering collaboration and ... Statistics, Mathematics, etc.) or equivalent degree and 6 or more years of experience; or any ...

... associates and suppliers to perform effective problems solving using standard tools (8D, 3P and ... Education Requirements: • Bachelor of Science/Arts in Engineering or related field / equivalent ...

... an Associate degree in supply chain, operations, logistics, business, or engineering. • 2+ years of relevant work experience in a similar role. • Strong knowledge of statistical forecasting ...

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Associate Statistical Programmer information

See Grayson, GA salary details

$78.4K

$136.7K

$231.1K

How much do associate statistical programmer jobs pay per year?

As of Jun 9, 2026, the average yearly pay for associate statistical programmer in Grayson, GA is $136,677.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,000.00 and $148,500.00 per year, depending on experience, location, and employer.

What is an Associate Statistical Programmer?

An Associate Statistical Programmer is an entry-level professional who assists in the programming and analysis of clinical trial data, primarily within the pharmaceutical or biotechnology industries. They use statistical software, such as SAS or R, to create, validate, and maintain datasets, tables, listings, and figures required for clinical study reports. Their work supports biostatisticians and clinical teams in ensuring data accuracy and regulatory compliance. This role is ideal for those with a background in statistics, mathematics, or computer science, looking to start a career in clinical data analysis.

How does an Associate Statistical Programmer typically collaborate with biostatisticians and data managers in clinical research projects?

As an Associate Statistical Programmer, you will frequently collaborate with biostatisticians to understand statistical analysis plans and translate them into clear programming specifications. You’ll also work closely with data managers to ensure data integrity and resolve any data discrepancies before analysis. Effective communication and teamwork are essential, as you’ll often participate in project meetings, provide programming support, and help deliver high-quality datasets and reports under tight timelines. This collaborative environment is key to ensuring accurate and timely clinical trial results.

What is the difference between Associate Statistical Programmer vs Statistical Programmer?

AspectAssociate Statistical ProgrammerStatistical Programmer
Required CredentialsBachelor's degree in statistics, mathematics, or related field; some roles may require basic programming skillsBachelor's or master's degree; more experience in programming and statistical analysis
Work EnvironmentEntry-level, supporting senior programmers; often in clinical research or pharmaceutical companiesMore independent, handling complex analyses; similar industry settings
Employer & Industry UsageCommon in clinical trials, pharmaceutical, and biotech companiesUsed across similar industries, often as a step up from associate roles

The main difference between an Associate Statistical Programmer and a Statistical Programmer lies in experience and responsibility level. Associate roles are typically entry-level, focusing on supporting tasks under supervision, while Statistical Programmers handle more complex analyses independently. Both roles are vital in clinical research and biotech industries, with the associate position serving as a stepping stone to more advanced programming roles.

What are the key skills and qualifications needed to thrive as an Associate Statistical Programmer, and why are they important?

To thrive as an Associate Statistical Programmer, you need a solid background in statistics, programming (especially SAS or R), and familiarity with clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Proficiency with statistical software (such as SAS, R, or Python), CDISC standards, and data management tools is essential, and certifications in SAS programming can be advantageous. Attention to detail, strong problem-solving abilities, and effective communication skills help you collaborate with clinical teams and ensure data quality. These skills and qualities are vital for delivering accurate statistical analyses that support regulatory submissions and evidence-based decision-making in clinical research.
Mgr, Quality / Lean

Mgr, Quality / Lean

Synventive Molding Solutions, Inc.

Lawrenceville, GA • On-site

Full-time

Posted 2 days ago


Job description

Core Responsibilities:

· Lead the expansion and sustainment of a committed quality culture throughout the entire value chain through influence and managing skills.

· Lead the translation of customer, industry, & regulatory requirements into appropriate manufacturing & inspection methods and transfer them into standard work to ensure quality is achieved in-house and at suppliers.

· Participate in new product development and/or introduction planning and execute quality actions to ensure smooth launch.

· Manage pre-production validation package for Customer approval: First Article Inspection (FAI).

· Lead containment, root cause analysis, corrective, and preventive actions (RCCA/CAPA); train and mentor other associates and suppliers to perform effective problems solving using standard tools (8D, 3P and 5Why, etc.).

· Manage the cost of quality to achieve business goals and optimize return on investment.

· Lead, participate in and facilitate cross-functional teams on process control and optimization projects to

stabilize and improve first passed yield; participate in other continuous improvement projects (i.e., Kaizen).

· Develop / refine advanced problem solving & process improvement methods & toolkit, and train employees in-house, and at Suppliers.

· Maintain strong communication with customers, internal management team and vendors to ensure quality level is meeting expectations.

· Develop Capital Acquisition Appropriation Request (CAAR) to support business needs.

· Manage development and performance of direct reports.

Qualifications:

· Proven ability to read and interpret drawings, GD&T requirements, and specifications. Then connect the technical requirements to appropriate manufacturing & inspection methods. Work with customers and suppliers to refine their processes.

· Excellent quantitative, statistical and analytical skills.

· Must be able to make timely decisions, set priorities, and execute plan to meet commitment: Customers’ business needs.

· Excellent interpersonal and communication skills; proven ability to effectively influence and motivate others; must be able to deal with ambiguity and various changing requirements.

· Proven functional experience in a manufacturing environment with successful track record of results.

· Proficient computer skills on Microsoft Word, Excel, and PowerPoint, and statistical tools.

· Minimum of 5 years’ experience in manufacturing.

Education Requirements:

· Bachelor of Science/Arts in Engineering or related field / equivalent degree; MBA, MS, or MA preferred (or equivalent).

· ASQ Certified Quality Engineer CQE, CMQ is preferred.

· Lead internal auditor per ISO 9001 preferred.