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Director Statistical Programming Jobs in Kansas (NOW HIRING)

Altasciences

Biostatistician II

Overland Park, KS · On-site +1

$70K - $90K/yr

Develop and quality control (QC) review statistical analysis for studies of simple to complex ... Oversee Preclinical projects and work with line manager to direct the activities of ...

New

Preco, LLC

Die Cutting Applications Engineer

Lenexa, KS · On-site

$70 - $90/hr

... self-directed work environment. * Team project driver to ensure progress milestones and on-time ... Knowledge of Microsoft office, computers, statistical analysis, and electrical basics will be ...

New

AXIUS GROUP LLC

CNC Machinist (2nd Shift)

Park City, KS · On-site

$18.25 - $25/hr

Read and follow blueprints, mylars, engineering orders, statistical process controls, planning ... Handle and dispose of hazardous waste and chemicals as directed and locate and use applicable ...

KODION ENERGY LLC

Quality Control Manager

Paola, KS · On-site

$45K - $75K/yr

They oversee the entire Quality Management System (QMS), direct inspection teams, and enforce ... Statistical Process Control (SPC). * Certifications: ASQ certifications (Certified Quality Engineer ...

KODION ENERGY LLC

Quality Control Manager

Paola, KS · On-site

$45K - $75K/yr

They oversee the entire Quality Management System (QMS), direct inspection teams, and enforce ... Statistical Process Control (SPC). * Certifications: ASQ certifications (Certified Quality Engineer ...

Merck & Co.

... in direct experience on the farm and in the clinic, we work hand in hand with our customers every ... process monitoring, statistical analysis, and data interpretationCore CompetenciesTechnical ...

DZConneX Solutions Ltd

Engineer, Quality 3

Parsons, KS · On-site

$81 - $121/hr

Provides direct Quality Engineering support to assigned programs. Plans and executes innovative, problem and defect prevention/process improvement methods. Applies statistics to problem solving and ...

New

MSD

Associate Specialist, Engineering

De Soto, KS

Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers ... Familiarity with process monitoring, statistical analysis, and data interpretation Core ...

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All JobsStatistical Programming JobsDirector Statistical Programming JobsDirector Statistical Programming Jobs in Kansas

Director Statistical Programming information

See Kansas salary details

$136.9K

$249.8K

$306.8K

How much do director statistical programming jobs pay per year?

As of Aug 21, 2026, the average yearly pay for director statistical programming in Kansas is $249,849.00, according to ZipRecruiter salary data. Most workers in this role earn between $232,300.00 and $287,600.00 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.
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Director Statistical Programming jobs near you
Infographic showing various Director Statistical Programming job openings in Kansas 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 $249,849 per year, or $120.1 per hour.

Biostatistician II

Altasciences

Overland Park, KS • On-site, Remote

$70K - $90K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 2 days ago

New

Altasciences rating

7.6

Company rating: 7.6 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

60th of 120 rated laboratories

Job description

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role
The Biostatistician II is responsible for having a working knowledge of all related processes with the ability to independently lead a study, support analysis, and provide high quality documents to support sponsors' research programs.
What You'll Do Here
  • Follow department and company standard operating procedures (SOPs), forms, templates and policies.
  • Act as Lead Biostatistician for simple to complex studies and be the central point of contact for the assigned Biostatistics team, extended internal project team and the client.
  • Provide input for Biostatistics portion of project timelines.
  • Review of protocols for simple to complex studies.
  • Generate randomization schedules using SAS or randomization specific software.
  • Develop and quality control (QC) review statistical analysis for studies of simple to complex including those involving safety data and pharmacokinetic (PK) or pharmacodynamic (PD) endpoints.
  • Develop or assist in developing the Statistical Analysis Plans (SAPs) and related table, figure, and listing (TFL) shells for studies of simple to moderate complexity.
  • Development of tables of summary statistics and graphics for clinical aspects of clinical trials.
  • Assist in answering deficiency letters from regulatory agencies, as required.
  • Utilize SAS to create and validate inferential statistical programs and results.
  • Perform QC review of analyses and documents prepared by other team members for completeness, accuracy, consistency, and structure.
  • Oversee Preclinical projects and work with line manager to direct the activities of Biostatisticians on assigned projects which include reviewing the protocol, results of statistical analyses, statistical report produced by other Biostatisticians, and providing support across all statistical tasks during the lifecycle of the project from protocol to final report.
  • Coordinate with internal team to deliver high-quality documents in accordance with the timelines agreed upon.
  • May represent Biostatistics in client and inter-departmental meetings.
  • Conduct all work in compliance with SOPs, Good Clinical Practice (GCP), and all regulatory guidelines.
  • Maintain familiarity with client and internal team expectations and produce analyses and documents consistent with these.
  • Have awareness of regulatory guidelines of related authorities (Therapeutic Products Directorate [TPD], FDA, European Medicines Agency [EMA], etc) as well as ICH and GCP procedures.
  • May participate or lead departmental or interdepartmental quality improvement initiatives.
  • Maintain and participate in the objectives of the department.
  • Other duties as assigned.

What You'll Need to Succeed
  • Bachelor's Degree or higher in Statistics or related field required.
  • Minimum of 2 Years of related experience preferred.
  • SAS, MS Word, Excel, Outlook, MS Teams, and Power Point.
  • Ability to read and interpret technical documents and industry specific manuals.
  • Ability to write advanced reports and correspondence.
  • Ability to speak effectively before groups of customers or employees of the organization.
  • Bilingual proficiency in French may be required, depending on location.
  • Excellent verbal and written communication skills.
  • Professional attitude and strong interpersonal skills.
  • Ability to work well with a multi-disciplinary team of professionals.
  • Client-focused approach to work.
  • Flexible attitude with respect to work assignments and new learning.
  • Ability to prioritize workload.
  • Superior attention to detail.
  • Understanding of clinical research project life cycle and applicable regulatory guidelines.
  • Good computer skills (Microsoft Word, Excel, and Power Point) and ability to understand and adapt to information technology (IT) systems as needed.
  • Moderate SAS programming proficiency.

What We Offer
The salary range estimated for this position is $70,000 - $90,000. Please note that salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data. Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences' Benefits Package Includes:
  • Health/Dental/Vision Insurance Plans
  • 401(k)/RRSP with Employer Match
  • Paid Vacation and Holidays
  • Paid Sick and Bereavement Leave
  • Employee Assistance & Telehealth Programs

Altasciences' Incentive Programs Include:
  • Training & Development Programs
  • Employee Referral Bonus Program
  • Annual Performance Review

#LI-MB1
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!

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