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Clinical Statistical Programmer Jobs in Oregon (NOW HIRING)

Natera

OR · On-site

As a Director, you will provide strategic and technical oversight for all statistical programming activities supporting the clinical validation and utility of Natera's cutting-edge molecular ...

Syneoshealth

OR

May be responsibleas Lead Biostatistician for the statistical aspects of the protocol, generation of randomization schedule, and input to the clinical study report. Creates or reviews programming ...

Spyre Therapeutics

OR · On-site

$290K/yr

... statistical programmer at a program level * Provide statistical input to strategic planning, study design, protocol development, sample size calculation, CRF, Results Interpretation, clinical study ...

Ultragenyx Pharmaceutical

Director, Biostatistics

OR · Remote

... statistical lead; provides technical leadership and biostatistical support on the design and conduct of clinical studies; participates in the evaluation, interpretation, and reporting of study ...

New

Parabilis Medicines

OR · On-site

The Vice President of Biometry will lead Parabilis's biometrics organization, overseeing biostatistics, statistical programming, data management, clinical data science and Real-World Data to support ...

DLH

OR · On-site

$50K - $80K/yr

Develop SAS programs for validating surveillance, clinical, or research study data. * Verify that ... Bachelor's degree in public health, statistics, or related field. * 2 years of experience working ...

Arcus Biosciences

$245K - $260K/yr

This includes design and execution of clinical pharmacology studies, design of clinical ... An advanced degree in Pharmaceutics/Pharmacy/Engineering/Statistics with demonstrated expertise in ...

Cotiviti

$125K - $172K/yr

Drive the data flywheel: convert expert clinician and auditor review decisions into high-quality ... PhD in a quantitative discipline such as Computer Science/Engineering, Statistics, Operations ...

New

Natera

OR

$126K - $166K/yr

The Clinical Genomics Engineering organization builds software that supports complex, regulated ... Bachelor's degree in life sciences, engineering, computer science, statistics, or equivalent ...

Syneos Health/ inVentiv Health Commercial LLC

OR · On-site

SME in Virology Clinical Trials *Requires graduate degree in Epidemiology, Statistics, or Public ... Requires basic knowledge of statistical programming language(s) (e.g., SAS, R, Python); *Excellent ...

New

Syneos Health/ inVentiv Health Commercial LLC

OR · On-site

SME in Oncology Clinical Trials *Requires graduate degree in Epidemiology, Statistics, or Public ... Requires basic knowledge of statistical programming language(s) (e.g., SAS, R, Python); *Excellent ...

New

OneStudyTeam

Senior Data Scientist

OR · On-site +1

$140K - $190K/yr

... for clinical trials. In this position, you will drive the development of statistical models and ... This role involves close collaboration with cross-functional teams (especially ML Engineering) to ...

ZEISS

Senior Advisor, Regulatory and Clinical Affairs

OR · Remote

$183K - $228K/yr

Master's degree with emphasis inthe PhysicalSciences, Mathematics, Statistics, or Engineering with a strong clinical foundationrequired.Stronglyprefer O.D., Ph.D. or M.D. * Thought leader in the ...

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Clinical Statistical Programmer information

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How much do clinical statistical programmer jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for clinical statistical programmer in Oregon is $57.28, according to ZipRecruiter salary data. Most workers in this role earn between $36.35 and $86.15 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Statistical Programmers when working with clinical trial data?

Clinical Statistical Programmers often encounter challenges such as handling large and complex datasets, ensuring data integrity, and adhering to strict regulatory guidelines (like CDISC standards). Collaborating closely with biostatisticians, data managers, and clinical teams is essential to resolve data discrepancies and meet tight project deadlines. Staying updated on evolving regulatory requirements and software tools is also vital to maintain high-quality deliverables in a fast-paced environment.

What are the key skills and qualifications needed to thrive as a Clinical Statistical Programmer, and why are they important?

To thrive as a Clinical Statistical Programmer, you need strong proficiency in statistical programming languages (such as SAS or R), a background in statistics or life sciences, and familiarity with clinical trial processes. Experience with CDISC standards (SDTM, ADaM), regulatory submission requirements, and version control systems is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills ensure the accurate analysis and reporting of clinical data, which is critical for regulatory compliance and successful clinical trial outcomes.

What does a Clinical Statistical Programmer do?

A Clinical Statistical Programmer is responsible for managing and analyzing clinical trial data using statistical software, such as SAS or R. Their primary tasks include creating datasets, programming statistical analyses, and generating tables, listings, and figures for clinical study reports. They work closely with biostatisticians and clinical research teams to ensure data accuracy and regulatory compliance. Their work is essential for supporting submissions to regulatory agencies and for making data-driven decisions in clinical research.

What Does a Clinical Statistical Programmer Do?

The job duties of a clinical statistical programmer involve collecting data, performing statistical analysis, and analyzing data sets according to the needs of their employer or client. Your responsibilities in this career may involve using SAS programming to create and analyze data sets during clinical trials or other clinical experiments and studies. You may also be involved in performing data integration for reports following clinical research or statistical analysis for quality control (QC).

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Clinical Statistical Programmer jobs near you
Director, Statistical Programming

Director, Statistical Programming

Mineralys Therapeutics

OR • Remote

$235K - $248K/yr

Other

Medical, Dental, Vision, Retirement

Re-posted 17 days ago

Job description

"Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone.  Its initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor.  Mineralys is headquartered in Radnor, Pennsylvania. For more information, please visit https://mineralystx.com. Follow Mineralys on LinkedIn, Twitter and Bluesky"

Mineralys is a fully remote company.

Director Statistical Programmer 

The Director Statistical Programing (SP) reports to the SVP, Biometrics and is accountable for the production of SDTM and ADAM datasets and Tables, Listings, and Graph output (TFLs) for clinical studies. They will collaborate with partner functions in the Clinical Development Department (e.g. Clinical Operations, Clinical Research, Biostatisticians). They will be accountable for Medical Affairs support by providing output for posters, presentations, and publications.

Key Responsibilities:

  • Accountable for all core SP deliverables (SDTM, ADAM, TFLs)
  • May also be accountable for clinical programming tasks (creation of SDTM and complex edit checks)
  • Provides ongoing data review by providing programmed edit checks, risk-based monitoring metrics, and draft TFLs
  • With IT, defines our programming environment and its validation
  • Responsible for the development of standards, SOPs, and best practices
  • The role is a combination of vendor oversight, supervision of more junior statistical programmers, and some hands-on work.
  • The Director SP will supervise assigned junior programmers, both contractors and regular staff members.

Qualifications

  • BS/BA degree and 10+ years of experience in analyzing clinical data OR
  • MS in statistics or related area and 7+ years of experience in analyzing clinical data.
  • Experience with FDA submissions and the provision of data submission packages
  • Experience in multiple areas outside of clinical development (e.g. pre-clinical, medical affairs, RWE)
  • Deep knowledge of the SAS programming language
  • Demonstrated accomplishments in automatization (usually through SAS macro development)
  • Working knowledge of at least one other programming language, preferably R
  • Experience with using genAI to create programming code or data processing algorithms.
  • Ability to work in an interdisciplinary team in a collaborative way
  • Represents biometrics in a positive and professional manner
  • Ability to work in a fast-paced team environment with fluctuating priorities
  • Common sense and solution-oriented mindset
  • Intellectual curiosity with a sense of pragmatic implementation of new ideas
  • Ability to communicate effectively in English, both orally and in writing.

Core Competencies

  • Strong understanding of clinical development processes and regulatory expectations
  • Ability to lead and influence in a matrixed environment
  • Demonstrated ability to balance urgency with quality
  • Analytical rigor with a pragmatic, execution-oriented mindset

Travel

  • This position requires up to 10% travel. Frequently travel is outside the local area and overnight.

This position is eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level.

US Salary Range:  $235,000 - $248,000

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