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Senior Statistical Programmer Jobs in Midland, GA

Senior Manager - Warehousing

Lagrange, GA · On-site

$128K - $192K/yr

... Engineering, Continuous Improvement work or related area. 4 years' experience leading teams. Knowledge and application of a functioning Quality Management System elements (for example, Statistical ...

In this role you will join the Quality Control Team and report to Quality Control Senior Manager ... Collaborate with engineering and production teams to identify and eliminate quality issues. * Lead ...

In this role you will join the Quality Control Team and report to Quality Control Senior Manager ... Collaborate with engineering and production teams to identify and eliminate quality issues. * Lead ...

In this role you will join the Quality Control Team and report to Quality Control Senior Manager ... Collaborate with engineering and production teams to identify and eliminate quality issues. * Lead ...

... Engineering, Continuous Improvement work or related area. 4 years' experience leading teams. Knowledge and application of a functioning Quality Management System elements (for example, Statistical ...

EH&S Manager

Columbus, GA · On-site

$72K - $98K/yr

Conducts EHS&S audits, documents statistics with respect to EHS&S program compliance, and makes ... As a resource to the management teams, provide feedback to senior management regarding feasibility ...

EH&S Manager

Columbus, GA · On-site

$72K - $98K/yr

Conducts EHS&S audits, documents statistics with respect to EHS&S program compliance, and makes ... As a resource to the management teams, provide feedback to senior management regarding feasibility ...

EH&S Manager

Columbus, GA

$72K - $98K/yr

Conducts EHS&S audits, documents statistics with respect to EHS&S program compliance, and makes ... As a resource to the management teams, provide feedback to senior management regarding feasibility ...

EH&S Manager

Columbus, GA · On-site

$74K - $100K/yr

Conducts EHS&S audits, documents statistics with respect to EHS&S program compliance, and makes ... As a resource to the management teams, provide feedback to senior management regarding feasibility ...

Senior Statistical Programmer information

See Midland, GA salary details

$74K

$115K

$150.1K

How much do senior statistical programmer jobs pay per year?

As of Sep 2, 2026, the average yearly pay for senior statistical programmer in Midland, GA is $115,000.00, according to ZipRecruiter salary data. Most workers in this role earn between $95,900.00 and $132,700.00 per year, depending on experience, location, and employer.

What is a senior statistical programmer?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

What are the typical responsibilities and team dynamics for a senior statistical programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

What are the key skills and qualifications needed to thrive as a senior statistical programmer, and why are they important?

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What cities near Midland, GA are hiring for Senior Statistical Programmer jobs?

Cities near Midland, GA with the most Senior Statistical Programmer job openings:

Sr. Process Controls & Validation Engineer

Regeneron Pharmaceuticals

Valley, AL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 11 hours ago


Regeneron rating

8.5

Company rating: 8.5 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

19th of 86 rated pharmaceutical


Job description

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We're seeking a Process Controls & Validation Engineer with a strong background in cGMP validation, who can develop sound process control strategy, bring structure to ambiguous technical problems, and confidently lead and influence discussions across Manufacturing, Quality and Regulatory teams. Process Sciences is a technical services department that deals with a range of scientific, technical, engineering and mathematical needs from the laboratory to the manufacturing floor. This role provides technical support to our bulk manufacturing, quality and CMC Regulatory for manufacturing processes from technology transfer and/or design transfer to post-commercial lifecycle management activities.

When & where:

  • Location: East Greenbush, New York, United States
  • Work Schedule: Monday-Friday, 8am-4:30pm

Discover your role:

  • Leads and provides hands-on support for cGMP process validation (Stage 1-3), technology transfer, design transfer, scale-up, and process control strategy development, from protocol authoring through execution and lifecycle management-translating ambiguous, early-stage problems into clear, actionable plans with limited direction
  • Evaluates product/process risk and applies engineering judgment to resolve gaps and uncertainty as processes move from development to at-scale manufacturing
  • Analyzes data across the process lifecycle-from development through characterization and manufacturing history-using statistics and engineering principles to inform control strategy, validation decisions, and identify critical process parameters, control limits, and monitoring plans
  • Leads and influences cross-functional discussions with Manufacturing, Quality Control, Quality Assurance, and CMC Regulatory, driving alignment and decisions on process lifecycle management, and effectively navigating differing stakeholder priorities
  • Authors protocols, reports, and technical documents grounded in available process/product knowledge; ensures SOPs, policies, and validation plans align with industry/regulatory expectations (e.g., ICH); supports audits/inspections and CMC sections of regulatory submissions as needed
  • Provides hands-on support for laboratory and manufacturing-scale studies, working effectively in a team-oriented environment

This role requires:

  • BS in Engineering; chemical engineering or biomedical engineering preferred
    • Process Controls & Validation Engineer: 2+ years of experience
    • Sr. Process Controls & Validation Engineer: 5+ years of experience
    • Level will be determined based on experience
  • Experience with process validation, tech transfer and scale up for drug substance

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.


Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

$67,400.00 - $128,700.00

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