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Director Statistical Programming Jobs in Fort Wayne, IN

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Director, Engineering

Fort Wayne, IN · On-site

$150 - $190/hr

The Engineering Director is responsible for manufacturing engineering activities and other critical ... Ability to work with mathematical concepts such as probability and statistical inference ...

The Engineering Director is responsible for manufacturing engineering activities and other critical ... and statistical inference, accounting and financial calculations and projections. Ability to ...

CMM Programmer

Albion, IN · On-site

  • Dental

  • Vision

  • Retirement

... providing statistical reports reflecting process control, process capability and gauge ... Ability to work independently (self-directed) and in a team-oriented environment. What Linamar Has ...

CMM Programmer

Albion, IN · On-site

  • Dental

  • Vision

  • Retirement

... providing statistical reports reflecting process control, process capability and gauge ... Ability to work independently (self-directed) and in a team-oriented environment. What Linamar Has ...

Resident Engineer

Fort Wayne, IN · On-site

$91K - $116K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Provide expert technical leadership in coordinating and directing cross functional teams in the ... Deliver statistical analysis of data on competition, customer direction, product performance ...

Solutions Engineer, Remote

Fort Wayne, IN · On-site

$120K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Partner with Sales Directors to identify customer business goals, needs, and pain points, and craft ... Strong analytical skills with expertise in Excel and statistical analysis. * Excellent ...

Senior Sterile Packaging Engineer

Larwill, IN · On-site

  • Medical

  • Dental

  • Vision

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

Senior Sterile Packaging Engineer

IN · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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

Manufacturing Engineer

Albion, IN · On-site

$66K - $85K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Self-directing a continuous improvement mentality for daily tasks. Computer Skills * Computer ... Familiarity with statistical analysis and software (Minitab / Cpk & Ppk) Communication Skills

Senior Engineer- Onsite

Fort Wayne, IN

$96K - $132K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... direct reports. * Research, acquire, evaluate, and validate fabricated or purchased equipment ... Create comparison reports and perform statistical analysis of equipment functions and of material ...

Quality Manager

Albion, IN

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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

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Director Statistical Programming information

See Fort Wayne, IN salary details

$151.5K

$276.4K

$339.4K

How much do director statistical programming jobs pay per year?

As of Aug 18, 2026, the average yearly pay for director statistical programming in Fort Wayne, IN is $276,408.00, according to ZipRecruiter salary data. Most workers in this role earn between $257,000.00 and $318,200.00 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 are popular job titles related to Director Statistical Programming jobs in Fort Wayne, IN?

For Director Statistical Programming jobs in Fort Wayne, IN, the most frequently searched job titles are:

What job categories do people searching Director Statistical Programming jobs in Fort Wayne, IN look for?

The top searched job categories for Director Statistical Programming jobs in Fort Wayne, IN are:

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

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

Infographic showing various Director Statistical Programming job openings in Fort Wayne, IN as of August 2026, with employment types broken down into 100% Full Time. Highlights an 69% In-person, 8% Hybrid, and 23% Remote job distribution, with an average salary of $276,408 per year, or $132.9 per hour.

Director of Biostatistics

micro1 AI

Fort Wayne, IN • Remote

$60 - $65/hr

Part-time

Posted 14 days ago


Job description

Role Title: Biostatistician


Role Type: Contractor


Location: Remote


micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review evaluation tasks that require deriving, reproducing, or validating statistical outputs from clinical datasets and associated tables, figures, and listings (TFLs).
  2. Apply expert judgment to assess the correctness and consistency of reported estimates, confidence intervals, p-values, analysis populations, and missing data handling in alignment with the statistical analysis plan (SAP).
  3. Identify discrepancies between statistical outputs and their narrative descriptions in clinical study reports (CSR), including subtle errors in population definitions, censoring rules, or multiplicity handling.
  4. Establish defensible ground truth for each evaluation task, documenting the derivation process to enable independent verification.
  5. Provide structured written rationales distinguishing true statistical errors from acceptable methodological alternatives, employing clear and concise communication.
  6. Collaborate with a multidisciplinary project team, providing statistical insights and feedback as needed to refine evaluation tasks and criteria.


Preferred Qualifications

  1. 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit.
  2. Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets.
  3. Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies under ICH E9(R1).
  4. Proficiency in SAS and/or R, with the ability to independently reproduce analyses from written specifications.
  5. Ability to interpret SAPs and ensure reported results are consistent with pre-specified analyses.
  6. Advanced degree (MSc or PhD) in Biostatistics, Statistics, or a closely related quantitative field.
  7. Nice to have: Experience as lead statistician on pivotal/registrational studies, authoring or reviewing CSR statistical sections, oncology endpoint expertise, and exposure to AI-assisted statistical review tools.