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Senior Statistical Programmer Jobs in Oregon (NOW HIRING)

... statistical programming, data management, clinical data science and Real-World Data to support ... Reporting to our SVP, Development Operations, the successful candidate will serve as a key member ...

AI Data Engineer Senior Consultant

Portland, OR · On-site

$121.40K - $145.80K/yr

They are seeking an AI Data Engineer Senior Consultant to build and operate the data, features, and ... Required : • Bachelor's degree in Computer Science, Engineering, Statistics, Data Science, or ...

New

$122.40K - $161.30K/yr

The Sr Software Engineer is primarily responsible for the performance and stability of critical ... statistical methods and models, and manipulating data using mathematical operations. * Data ...

Senior Quality Engineer

Hillsboro, OR · On-site

$96.40K - $130.70K/yr

Job Scope A Senior NPI Quality Engineer is responsible for quality planning and the overall quality ... Knowledge of quality and statistical analysis tools (e.g. SPC, 6 Sigma, Risk Analysis, FMEA, DOE ...

Senior Quality Engineer

Hillsboro, OR

$96.40K - $130.70K/yr

Job Scope A Senior NPI Quality Engineer is responsible for quality planning and the overall quality ... Knowledge of quality and statistical analysis tools (e.g. SPC, 6 Sigma, Risk Analysis, FMEA, DOE ...

Senior Data Scientist

OR · On-site +1

The contractor shall design and implement advanced ML models and statistical methods to optimize ... engineering processes, and audit compliance. * The contractor shall implement sprint-based Agile ...

The contractor shall design and implement advanced ML models and statistical methods to optimize ... engineering processes, and audit compliance. * The contractor shall implement sprint-based Agile ...

The contractor shall design and implement advanced ML models and statistical methods to optimize ... engineering processes, and audit compliance. * The contractor shall implement sprint-based Agile ...

The Senior Associate, Clinical Programming (EDC) will be responsible for overseeing all aspects of ... Work collaboratively with Programming (Clinical and Statistical) Clinical Operations, Biostatistics ...

As the Senior Engineering Manager on the team for Marketplace Optimization, you will lead high ... Background in statistics, economics, or applied ML domains * Demonstrated success building ...

Senior Machine Learning Engineer

OR · On-site +1

$140K - $190K/yr

By joining our team as a Senior Machine Learning Engineer , you will play a pivotal role in ... statistical modeling. Familiarity with NLP and large language models is important. * Analytical ...

As a Senior Engineer, Field Process, you will help expand ASM's advanced film technologies at our ... Experience designing, running, and interpreting DOEs or statistical experiments in academic ...

Sr. Electrical Engineer

Wilsonville, OR · On-site

$111.20K - $144.80K/yr

ESS Inc. is seeking a Sr. Electrical Engineer - Battery Energy Storage Systems (BESS) to lead and ... Proficiency in test planning, experimental design, and statistical data analysis for subscale and ...

Sr. Electrical Engineer

Wilsonville, OR · On-site

$111.20K - $144.80K/yr

ESS Inc. is seeking a Sr. Electrical Engineer - Battery Energy Storage Systems (BESS) to lead and ... Proficiency in test planning, experimental design, and statistical data analysis for subscale and ...

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Senior Statistical Programmer information

See Oregon salary details

$87.2K

$135.6K

$177.1K

How much do senior statistical programmer jobs pay per year?

As of May 29, 2026, the average yearly pay for senior statistical programmer in Oregon is $135,643.00, according to ZipRecruiter salary data. Most workers in this role earn between $113,100.00 and $156,500.00 per year, depending on experience, location, and employer.

What is a Senior Statistical Programmer job?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

What are the key skills and qualifications needed to thrive in the Senior Statistical Programmer position, and why are they important?

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are the typical responsibilities and team dynamics for a Senior Statistical Programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.
What are the most commonly searched types of Statistical Programmer jobs in Oregon? The most popular types of Statistical Programmer jobs in Oregon are:
What are popular job titles related to Senior Statistical Programmer jobs in Oregon? For Senior Statistical Programmer jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Senior Statistical Programmer jobs in Oregon look for? The top searched job categories for Senior Statistical Programmer jobs in Oregon are:
What cities in Oregon are hiring for Senior Statistical Programmer jobs? Cities in Oregon with the most Senior Statistical Programmer job openings:
Infographic showing various Senior Statistical Programmer job openings in Oregon as of May 2026, with employment types broken down into 5% As Needed, 83% Full Time, 9% Part Time, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $135,643 per year, or $65.2 per hour.

Other

Posted 26 days ago


Job description

Why Join Us?

As a member of the Parabilis Medicines team, you will be a part of an organization dedicated to creating extraordinary medicines for diseases with urgent unmet needs, harnessing our proprietary peptide platform to transform treatment possibilities for patients. Parabilis is a clinical-stage biopharmaceutical company dedicated to unlocking high-impact protein targets long-considered undruggable. The company has developed a new class of stabilized, cell-penetrant alpha-helical peptides - Helicons - capable of modulating intracellular proteins that are inaccessible to traditional drug modalities. 

Headquartered in Cambridge, Mass., Parabilis is advancing a focused pipeline of multiple first-in-class therapies across both rare and common cancers. Its lead asset, zolucatetide (FOG-001), is a first-in-class, clinically validated direct inhibitor of the interaction between -catenin and the T-cell factor (TCF) family of transcription factors, implicated in millions of cancer cases annually, including in colorectal cancer, desmoid tumors, hepatocellular carcinoma and a range of other Wnt/-catenin-driven tumors. In Phase 1 clinical trials, zolucatetide produced the first-ever clinical evidence that it can directly inhibit this interaction, once previously considered "undruggable" despite its role across multiple cancer types. Parabilis is also advancing investigational degraders of ERG and ARON into clinical development for the treatment of prostate cancer, as well as progressing other preclinical programs. Backed by a recent $305 million Series F financing, Parabilis is entering an exciting phase of growth and execution.

What's the opportunity?

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 clinical development programs from early-phase through regulatory submission. This strategic role ensures the integrity, quality, and compliance of all clinical trial data and analyses while driving innovation in data strategy and statistical methodologies. Reporting to our SVP, Development Operations, the successful candidate will serve as a key member of the Development leadership team, partnering closely with Clinical Development, Clinical Operations, Regulatory Affairs, translational/computational biology and other functions to enable data-driven decision-making and successful product development.

  • Lead and develop the Biometrics organization, including biostatistics, programming, data management Clinical Data science ensuring high-quality deliverables across all clinical programs and fostering a culture of scientific rigor, accountability, collaboration and innovation.
  • Oversee design and implementation of statistical methodologies for clinical trials.
  • Champion innovative methodologies, including adaptive and model-based approaches, to support efficient and agile drug development.
  • Provide strategic input into drug development strategies in collaboration with program-level and functional leadership, working closely with Clinical Development, Clinical Operations, and Translational Medicine.
  • Ensure the integrity, high quality and traceability of clinical trial data and the accuracy of all statistical analyses, leading to compliant deliverables in biometry.
  • Lead and support biometrics interactions with global health authorities.
  • Establish and maintain vendor partnerships ensuring quality and timely delivery of outsources biometrics activities.

What you'll need to be successful:

  • Doctoral degree in Biostatistics or related field.
  • 15+ years of biometrics experience within the biotech or pharmaceutical field.
  • Proven track record of leading, building, and managing teams.
  • Demonstrated record of fostering creativity, productivity, and execution with urgency, teamwork and accountability.
  • Company leader who leads by example, employs expertise and influence to encourage collaboration across departments, levels, and groups to achieve key objectives.
  • Deep knowledge of clinical trial design, regulatory requirements, and statistical environment.
  • Excellent problem-solving skills, strategic thinking, and ability to work in a fast-paced, collaborative environment.
  • Outstanding interpersonal skills, self-awareness, and ability to manage team dynamics.
  • Ideally, has worked in more than one therapeutic area and has direct experience with innovative Phase 1-3 clinical study designs for oncology.
  • Comfort with model-based drug development and agile drug development is important.
  • Appreciation for observational methodologies is preferred.
  • Ability to articulate complex methodologies to senior executives for their understanding is required with previous experience with presenting to senior executives being ideal.
  • Demonstrated use of AI tools in your current role and responsibilities is required. Advanced or innovated use of AI is a strong plus.

Core Values

Parabilis is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for all employees across the business, in all departments, and driving innovation for patient benefit.

  • Growth-Minded. We're inventing a new class of medicines-one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable.
  • In(ter)dependent.We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options.
  • Patient-focused.We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact.
  • All-In.We're All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history.

The base salary target for this position is $340,000-$380,000 per year, depending on experience, qualifications, and internal practices. Parabilis's total compensation package also includes an annual target bonus, equity, and a comprehensive suite of competitive benefits designed to support our employees' overall well-being.

As an equal opportunity employer, Parabilis values an inclusive workplace and welcomes applicants of all backgrounds and experiences. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.

30 Acorn Park Drive    |     Cambridge, MA 02140    |    www.parabilismed.com