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Director Statistical Programming Jobs in Nebraska

Senior Proccess Engineer

Omaha, NE · On-site

$99K - $128K/yr

Proven ability to manage technical projects through development and scale-up, with direct ... Strong proficiency with process modeling software (e.g., ASPEN+, SuperPro Designer) and statistical ...

Senior Proccess Engineer

Omaha, NE · On-site

$99K - $128K/yr

Proven ability to manage technical projects through development and scale-up, with direct ... Strong proficiency with process modeling software (e.g., ASPEN+, SuperPro Designer) and statistical ...

Quality Engineer

Holdrege, NE · On-site

$86K - $111K/yr

SUMMARY As directed by the Quality Engineering Manager, the Quality Engineer II is accountable for ... Demonstrate success with statistical and problem‑solving methodologies. * Excellent knowledge of ...

Front-End Developer, Craftsman

Omaha, NE · On-site

$99K - $115K/yr

Familiarity with querying external databases via Application Programming Interfaces (APIs) and ... Direct experience supporting USSTRATCOM, Combatant Command, or Department of Defense analytics ...

Front-End Developer, Craftsman

Omaha, NE · On-site

$99K - $115K/yr

Familiarity with querying external databases via Application Programming Interfaces (APIs) and ... Direct experience supporting USSTRATCOM, Combatant Command, or Department of Defense analytics ...

May require direct customer communication to negotiate changes to product designs or requirements ... Statistical Process Control) • Knowledge of measurement equipment and methods: CMM, Faro or Romer ...

Showing results 21-40

Director Statistical Programming information

See Nebraska salary details

$146.4K

$267.1K

$328K

How much do director statistical programming jobs pay per year?

As of Sep 11, 2026, the average yearly pay for director statistical programming in Nebraska is $267,106.00, according to ZipRecruiter salary data. Most workers in this role earn between $248,400.00 and $307,500.00 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 job categories do people searching Director Statistical Programming jobs in Nebraska look for?

The top searched job categories for Director Statistical Programming jobs in Nebraska are:

Senior Proccess Engineer

Omaha, NE • On-site

Bluestem Biosciences
Biotechnology Research and Development • 1 - 10 employees

$99K - $128K/yr

Full-time

Re-posted 25 days ago


Job description

ABOUT US:

We use American corn and existing bioethanol infrastructure to produce critical chemicals right here at home-powering U.S. competitiveness and securing our nation's supply chains - while reinvesting in agricultural America. Bluestem Biosciences has engineered a breakthrough in American manufacturing. Our proprietary biomanufacturing process represents a new, cost-effective, and advantaged way to produce platform chemicals domestically. With the foundation of existing infrastructure, we convert abundant, renewable American corn into high-value chemicals at scale. JOIN US AS WE ACCELERATE TO COMMERCIALIZATION

Role Summary

We are seeking an experienced chemical engineer to execute key process development efforts for the separation and purification of our target molecules. As the 'technical arm' of the Process Design & Operations team, this position reports directly to the VP, Process Design & Operations. Our ideal candidate will have practical, hands-on experience developing and scaling up bioindustrial separation processes. You will be responsible for designing and executing bench and pilot-scale experiments, analyzing process data, and building the techno-economic models that inform our scale-up strategy. You will collaborate closely with our internal strain design and fermentation teams and support the VP in managing technical collaborations with external engineering partners and CROs to drive the development and commercialization of our process.

Responsibilities
  • Design and conduct bench and pilot-scale process trials for downstream processing steps, including separation, purification, and waste management.
  • Execute and the process scale-up strategy, designing and executing experiments that advance the technology readiness level (TRL) to pre-commercial demonstration (TRL 7).
  • Analyze and interpret data from process trials to inform process intensification, improvement, and scale-up strategies.
  • Build and refine techno-economic models throughout the process development lifecycle to support the continuous refinement of Bluestem's integrated plant designs.
  • Provide hands-on expertise in a range of downstream unit operations, particularly filtration, ion exchange, and other separation techniques, while also supporting the development of distillation processes.
  • Collaborate closely with R&D (strain design and fermentation) to integrate upstream, downstream, and recycle streams, ensuring efficient and sustainable overall process performance.
  • Serve as the primary technical point of contact for projects with external lab, pilot, and CRO partners, managing day-to-day experimental execution and data transfer.
  • Provide the technical data package (e.g., mass balances, experimental results) to support the VP and engineering firms in translating processes into PFDs, P&IDs, and FEL packages.
  • Identify and interface with vendors and equipment suppliers for the design, procurement, and commissioning of downstream process equipment.
  • Align process development with existing manufacturing capabilities, designing with the 'end in mind'
Requirements
  • Advanced degree in Chemical Engineering, Process Engineering, or a related field, plus 8+ years of progressive experience in a process development or production engineering position.
  • Differing combinations of experience and education will be considered.
  • Demonstrated hands-on experience in DSP engineering principles and practice, with a strong understanding of chemical and biochemical fundamentals that drive optimal DSP design for fermented products.
  • Proven ability to manage technical projects through development and scale-up, with direct experience advancing technologies from bench/pilot to pre-commercial TRLs (TRL 7).
  • Direct experience with process scale-up, including identifying and mitigating risks, and translating lab-scale processes to pilot and demonstration scale equipment.
  • Strong proficiency with process modeling software (e.g., ASPEN+, SuperPro Designer) and statistical software (e.g., JMP, R, Python) to build models and analyze experimental data.
  • A strong understanding of upstream fermentation processes and how they impact downstream purification is essential for effective cross-functional collaboration.
  • Expertise with formal process and manufacturing engineering practices, such as statistical process control and continuous process improvement principles.
  • Strong communication skills, both written and verbal; organizational skills and ability to work in a dynamic and fast-paced environment.

Bluestem is an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.

Employment Type: FULL_TIME