What Sr Statistical Programmer Jobs are in the United States?

We are looking for a Sr Statistical Programmer to support a biotech client of ours in Seattle, WA. Interested candidates must have 5+ years of experience in statistical programming for clinical research trials.

Details:

• 6+ month contract
• Pay: $75hr OBO

Overview

The Senior Statistical Programmer provides advanced programming support and leads complex data analysis projects. This role develops and validates statistical programs, conducts quality control checks on data and analysis outputs, and optimizes programming processes and methodologies to ensure accuracy, efficiency, and compliance.

Responsibilities

• Develop and validate complex statistical programs.
• Conduct quality control checks on datasets and analysis outputs.
• Optimize programming processes and methodologies to improve efficiency.
• Lead complex data analysis projects, collaborating with statisticians and data managers to ensure accuracy.
• Document programming activities and maintain version control.
• Provide technical guidance and mentorship to junior programmers.
• Ensure compliance with regulatory requirements and industry standards.
• Troubleshoot and resolve programming issues.

Required Qualifications

• Bachelor’s degree in Statistics, Biostatistics, Computer Science, or a related field.
• 4+ years of experience in statistical programming.
• Proficiency in SAS, R, or Python.

Preferred Qualifications

• Experience in clinical trials or research studies.
• Knowledge of CDISC standards (SDTM, ADaM).

Knowledge, Skills, and Abilities

• Strong programming and problem-solving skills.
• Attention to detail and ability to perform rigorous quality checks.
• Effective communication and collaboration skills to work cross-functionally.
• Ability to lead projects and provide mentorship.

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Merck is seeking an Associate Principal Scientist in Statistical Programming located in Rahway, NJ. The role involves providing high-quality statistical programming analysis for Oncology projects and collaborating with teams to develop modeling datasets and reporting deliverables.

The ideal candidate will have extensive SAS programming experience and a Bachelor's or Master's degree in a relevant field. Merck offers a competitive salary range and comprehensive benefits including medical, dental, and vacation.

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Cytel Inc. is seeking an R Technical Solutions Programmer to implement the vision for data and analysis infrastructure platforms, supporting the data flow from collection to submission.

This role relies on R programming and clinical trials experience to build open‑source solutions for programming and analytics. You will collaborate with internal teams, develop reusable R code and documentation, and promote innovation in data analysis and visualization within regulated environments.

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MMS is seeking a Statistical Programmer to join our team in Canton Charter Township, MI. This role demands a Master's degree in Statistics and a minimum of 5 years of relevant experience, with mastery in SAS programming and strong communication skills.

The ideal candidate will have a proven track record in clinical trial data management and be familiar with FDA and GCP requirements. Join us at MMS, where contributions matter and the work environment nurtures innovation and collaboration.

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Kodiak Sciences Inc. is seeking an experienced Clinical Programmer to support statistical programming across multiple clinical studies.

The role involves writing, testing and validating SAS programs to create analysis datasets, TLFs, and other outputs for regulatory submissions and publications. You will collaborate with statisticians, data managers, medical writers, and clinical operations to meet programming deliverables, review vendor outputs, and contribute to SOP development in a

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A biotech consulting firm in Seattle is looking for a Senior Statistical Programmer to support clinical research trials. Candidates should have over 5 years of experience in statistical programming and be proficient in SAS, R, or Python. Responsibilities include developing statistical programs, conducting quality control checks, and leading data analysis projects. This is a 6+ month contract paying $75/hr.
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A leading CRO in the pharmaceutical sector is seeking a skilled statistical programmer for a mid-senior level role. The candidate will lead the development of CDISC-compliant datasets for CNS clinical trials, ensure accuracy of programming deliverables, and mentor junior team members. A bachelor's or master's degree in a relevant field and over 5 years of experience in statistical programming are required. This is a contract position based in Colorado, offering a fully remote setup.
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Adecco is currently assisting a local Customer in their search for a Sr Programmer Analyst positions in Irvine, CA This is a great opportunity to further your existing skills as a Sr Programmer Analyst, while learning new ones to assist you in your career. The best part is you would be joining a winning culture with Adecco while on assignment with our customer and have access to all our Adecco Perks!
Perks:
+ Shift: MON-FRI 08:00AM-5:00PM (with option to be hybrid)
+ Pay: $57.55 p/h
+ **Candidate must be located in Irvine, CA or near**
+ Access to Adecco's Aspire Academy ( with thousands of free upskilling courses
Responsibilities
+ Administer, support, and maintain Oracle EPM Cloud applications, including Planning, Financial Performance Management, EDM, Shared Services, and Narrative Reporting.
+ Develop and maintain Essbase BSO and ASO cubes, Planning applications, business rules, calculation scripts, forms, reports, and SmartView solutions.
+ Troubleshoot system, data, reporting, and cube issues, perform root cause analysis, and implement corrective actions.
+ Manage data integrations and data loads from SQL databases, Oracle applications, flat files, and other enterprise systems.
+ Create and maintain automation scripts, scheduled jobs, security roles, security filters, and OCI Identity Management configurations.
+ Gather business requirements, document solutions, develop test plans, and lead testing and User Acceptance Testing (UAT).
+ Provide technical leadership, drive system enhancements, support users, and track project deliverables through Jira.
Requirements
+ Bachelor's degree in Computer Science, Information Systems, or a related field (Master's preferred).
+ 8+ years of experience in IT application development, programming, or enterprise systems support.
+ 5+ years of hands-on experience with Oracle EPM Cloud (Oracle Enterprise Performance Management).
+ Strong experience with Oracle Planning, Essbase (BSO/ASO), Shared Services, EDM, and Narrative Reporting.
+ Experience developing Business Rules, Calc Scripts, Groovy scripts, SmartView reports, and Oracle EPM reporting solutions.
+ Knowledge of financial planning, budgeting, forecasting, consolidation, and enterprise reporting processes.
+ Excellent troubleshooting, communication, stakeholder management, and project leadership skills.
This role is being recruited for by one of our Centralized Delivery Team and not your local Branch. To be considered, please follow the steps included upon your application. For instant consideration for this Sr Programmer Analyst position with Adecco in Irvine, CA, apply today
**Pay Details:** $57.55 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
+ The California Fair Chance Act
+ Los Angeles City Fair Chance Ordinance
+ Los Angeles County Fair Chance Ordinance for Employers
+ San Francisco Fair Chance Ordinance
**Massachusetts Candidates Only:** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Statistical Programmer

Join to apply for the Statistical Programmer role at Katalyst CRO

Requirements

• B.Sc., M.Sc., or equivalent education in Biostatistics/Statistics, Bioinformatics, Life Sciences, Mathematics, Physical Sciences, or related fields
• Advanced SAS macro programming experience is required for the development of global tools that will increase the efficiency and capacity of the Statistical Programming group
• At least 6 years of Clinical trials related work experience in SAS programming, analysis and reporting in the context of drug development projects is required
• Well experienced in Pinnacle21 validation process, generating define xml using Pinnacle 21
• Extensive experience in implementing CDISC standards, as well as annotating CRFs, creating specifications for SDTM and ADaM datasets
• Experienced in creating Define.xml and the corresponding Reviewers' Guide for SDTM and ADaM datasets
• Good verbal and written communications skills in English
• Demonstrated knowledge of clinical drug development
• Proficiency in conducting advanced statistical analyses
• Must be independent, attention to detail, accountable to quality and timely delivery
• Ability to work on multiple collaborative projects, team player mentality

Responsibilities

• As a Statistical Programming Consultant, you will use your SAS and R programming skills to prepare SDTM and ADaM datasets, Tables, Listings, & Figures (TLFs), as well as create related documents such as aCRF, programming specifications, and define packages (including reviewer's guides) for Phase 1 to Phase 4 clinical trials
• In addition, you will conduct quality control and quality assurance activities on datasets and outputs and may participate in company initiatives to improve the efficiency of end-to-end statistical programming activities, analysis, and reporting (IT, methodology, automation, quality)
• You will work closely in teams led by statistical programmers, statisticians, and drug development consultants, supporting a variety of client projects across various therapeutic areas and complexities

Seniority level

• Mid-Senior level

Employment type

• Contract

Job function

• Information Technology
• Pharmaceutical Manufacturing

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