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Director Statistical Programming Jobs in Warsaw, IN

Manufacturing Engineer

Pierceton, IN

$67K - $87K/yr

Will also direct personnel to work with operations and regulatory teams to ensure processes are ... process control methods, statistical analysis, DOE, ISO standards and FDA quality system ...

Manufacturing Engineer

Pierceton, IN · On-site

$67K - $87K/yr

Will also direct personnel to work with operations and regulatory teams to ensure processes are ... process control methods, statistical analysis, DOE, ISO standards and FDA quality system ...

Manufacturing Engineer

Pierceton, IN · On-site

$67K - $87K/yr

Will also direct personnel to work with operations and regulatory teams to ensure processes are ... process control methods, statistical analysis, DOE, ISO standards and FDA quality system ...

Senior Quality Engineer

Plymouth, IN · On-site

$80K - $109K/yr

Managing Direct Reports * Developing and implementing quality control procedures and guidelines ... Experience with Statistical Software * Experience with Gage Repeatability and Reproducibility

Senior Quality Engineer

Plymouth, IN · On-site

$80K - $109K/yr

Managing Direct Reports * Developing and implementing quality control procedures and guidelines ... Experience with Statistical Software * Experience with Gage Repeatability and Reproducibility

While this role has no direct supervisory responsibility, it mentors engineers and technical staff ... Experience with manufacturing processes, process validation, statistical analysis, and risk ...

While this role has no direct supervisory responsibility, it mentors engineers and technical staff ... Experience with manufacturing processes, process validation, statistical analysis, and risk ...

... engineering, production, and supply chain teams. Key responsibilities include ... Planning and directing quality control, quality assurance, and continuous improvement initiatives

Bachelor's degree in Packaging Engineering, Packaging Science, Engineering, or related technical ... Experience with manufacturing processes, process validation, statistical analysis, and risk ...

Bachelor's degree in Packaging Engineering, Packaging Science, Engineering, or related technical ... Experience with manufacturing processes, process validation, statistical analysis, and risk ...

Director Statistical Programming information

See Warsaw, IN salary details

$148K

$270.1K

$331.7K

How much do director statistical programming jobs pay per year?

As of Sep 10, 2026, the average yearly pay for director statistical programming in Warsaw, IN is $270,104.00, according to ZipRecruiter salary data. Most workers in this role earn between $251,200.00 and $310,900.00 per year, depending on experience, location, and employer.

What is a director statistical programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

What does a director statistical programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.

What are the key skills and qualifications needed to thrive as a director statistical programming?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

How does a director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What cities near Warsaw, IN are hiring for Director Statistical Programming jobs?

Cities near Warsaw, IN with the most Director Statistical Programming job openings:

Senior Quality Engineer

Plymouth, IN

$80K - $109K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 13 days ago


Job description

Build More Than a Job-Build a Career at SpiTrex CTE

At SpiTrex CTE, we invest in our people. You'll find opportunities to grow, real flexibility, and a culture that values balance, development, and teamwork.


Why join CTE?

  • Career Growth:Ongoing training and development through Bamboo Path Track & WorkForge
  • Flexibility:Flextime options that support real life
  • Culture:Team events, Donut Fridays, food trucks, and more
  • Rewards:Referral bonuses, quarterly bonuses, and a 401(k) with 50% company match (up to 10%)
  • Benefits:No-cost vision, life, and short-term disability; dental & medical with HSA or PPO options


Ready to grow with a company that values you?Join SpiTrex CTE.


1st Shift: Monday to Thursday, 6AM - 3PM; Friday, 6AM - 10AM


Essential Functions:

  • Assisting with Customer Audits, Internal Audits, Notified Body Audits, and FDA Inspections
  • Assisting with Supplier Management (including but not limited to supplier performance review, and supplier audits)
  • Managing Direct Reports
  • Developing and implementing quality control procedures and guidelines
  • Monitoring and analyzing data to identify areas for improvement
  • Initiate quality improvement projects
  • Collaborate with cross-functional teams to resolve quality issues
  • Conducting audits on products and processes
  • Providing guidance to other team members
  • Investigating and resolving customer complaints
  • Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements
  • Reviewing and approving product and process changes
  • Developing procedures and work instructions as needed
  • Other work-related tasks as assigned


Competency:

  • Strong background in quality control and quality engineering functions
  • Understanding GD&T
  • Experience with Statistical Software
  • Experience with Gage Repeatability and Reproducibility
  • Excellent communication skills
  • Excellent leadership skills
  • Detail-oriented
  • Strong analytical and problem-solving skills
  • Ability to manage multiple projects simultaneously
  • Strong understanding of medical device regulations


Educational Requirements:

B.S. in Engineering field preferred or minimum of 5 years in Quality Engineering role


Experience:

5-7 years of Medical Device experience in Quality setting preferred


Benefits Include:

  • Medical, Vision and Dental Insurance
  • Short-Term Disability
  • Life Insurance
  • 401(k) - 50% company match (up to 10% contribution)
  • Paid vacation days
  • Paid holidays