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Director Statistical Programming Jobs in Indiana

Steuben County

Executive Director

Angola, IN · On-site

Develops and manages budget and grants, oversees Project Income fund, creates statistical reports ... and adjusting programming and policies as needed. Oversees documentation of all violations.

General Motors

Dimensional Engineer

Roanoke, IN · On-site

This includes direct company sponsorship, entry of GM as the immigration employer of record on a ... Drives variation reductions utilizing Statistical Process Control methodology * Ensures full ...

General Motors

Dimensional Engineer

Roanoke, IN · On-site

This includes direct company sponsorship, entry of GM as the immigration employer of record on a ... Drives variation reductions utilizing Statistical Process Control methodology * Ensures full ...

Welbilt

Quality Engineer II (50205)

New Albany, IN · On-site

$66K - $86K/yr

Under direct supervision, this position is responsible for ensuring the quality of processes and ... Knowledgeable and proficient in the use of statistical software for process and product analysis.

Welbilt

Quality Engineer II (50205)

New Albany, IN

$66K - $86K/yr

Under direct supervision, this position is responsible for ensuring the quality of processes and ... Knowledgeable and proficient in the use of statistical software for process and product analysis.

Samtec, Inc

Cable Process Engineer

New Albany, IN · On-site

This is an opportunity to make a direct impact on the development and optimization of advanced ... Analyze manufacturing data using statistical tools and software such as Minitab and Excel to ...

New

samtec

Cable Process Engineer

New Albany, IN · On-site

This is an opportunity to make a direct impact on the development and optimization of advanced ... Analyze manufacturing data using statistical tools and software such as Minitab and Excel to ...

New

Samtec, Inc

Cable Process Engineer

New Albany, IN · On-site

This is an opportunity to make a direct impact on the development and optimization of advanced ... Analyze manufacturing data using statistical tools and software such as Minitab and Excel to ...

New

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All JobsStatistical Programming JobsDirector Statistical Programming JobsDirector Statistical Programming Jobs in Indiana

Director Statistical Programming information

See Indiana salary details

$146.1K

$266.6K

$327.3K

How much do director statistical programming jobs pay per year?

As of Jul 8, 2026, the average yearly pay for director statistical programming in Indiana is $266,578.00, according to ZipRecruiter salary data. Most workers in this role earn between $247,900.00 and $306,900.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Director of Statistical Programming, and why are they important?

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.

What Is the Job of 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.

How does a Director of 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 does a Director of 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.
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Director Statistical Programming jobs near you
Quality Engineers On W2 Only

Quality Engineers On W2 Only

Sovereign Technologies

Warsaw, IN • On-site

$60K - $78K/yr

Other

Posted 8 days ago

Job description

Title : Quality Engineers
Location : Warsaw, Indiana
Duration : 12 Months
Rate : Open

Relevant Experience: 10+ Years

Primary Role
Provide lead quality support for New Product Development Teams to ensure new/improved medical device products and processes are in compliance with applicable standards and regulations. Responsible design quality to ensure compliance to design control systems. Plan and lead projects by identifying and organizing activities into time dependent sequencing with realistic timelines. Work effectively/ productively with all departments by developing a team atmosphere.

Key Responsibility

  • Assist all elements of the design control system and DHF creation from a design quality perspective for new product development
  • Help execute within a QA system and team that ensures alignment to the Balmoral QMS while optimizing time to regulatory approval/clearance
  • Work with suppliers to review and drive the following to ensure regulatory clearance and production readiness: engineering drawing review, gage development, capability studies, gage RRs, special process validations, tolerance stackups, CMM correlation studies, PFMEa, Process flows, control plans, inspection plans, DHR reviews.
  • Develops and implements corrective/preventative action plans, internal CAPA s and supplier SCARs
  • Provide verification and validation, sampling, and statistical analysis support for all functions required for product clearance/approval through supplier relationships(eg mechanical testing, manufacturing special processes, packaging, sterilization)
  • Design and implement inspection methods, equipment, acceptance criteria and sampling plans to support qualified vendors

Qualification

  • Knowledge of design control requirements per ISO 13485 and 21 CFR part 820
  • Quality system regulations and requirements (i.e. 21 CFR part 820, ISO 13485, ISO 9001, ISO 14971)
  • Problem solving using root cause methodologies (i.e. DMAIC, The Shainin System, Ishikawa)
  • Knowledge of statistics, process control, and process capability
  • Applying statistics and software in data analysis (example Minitab)
  • Application of Risk management ISO 14971 and failure modes and effects analysis (FMEA)
  • Use of Computer Aided Drafting Software package (i.e. NX, Solidworks)
  • Geometric Dimensioning and tolerancing (GD&T)
  • Inspection methods and limitations based on engineering drawings and associated tolerances
  • Ability to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).
  • Able to communicate both orally and in written form to multiple levels of the company.
  • BS in engineering or an alternative Bachelor s degree program
  • 3+ years experience in an Orthopedic Quality Engineering role
  • Combination of education and experience may be considered relative to requirements
Travel Requirements
20% travel may be required
Regards,

Shanthi Pedhiredla

SOVEREIGN TECHNOLOGIES LLC

Desk no - # 4
Direct no - ()
Certified Minority Owned Business ( MBE)

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