ZipRecruiter

Log In

1

Senior Statistical Programmer Jobs in Berkeley, CA

Gilead

Sr Manager, Statistical Programming

Foster City, CA · On-site

$169K - $219K/yr

We are in search of a Sr Manager, Statistical Programming to join our team! Statistical Programming- Analysis Programming: Statistical programmers work collaboratively with internal colleagues and ...

Erasca

SVP Biometrics

San Francisco, CA · On-site

This includes leadership of the Biostatistics, Statistical Programming & Analysis, and Clinical ... In collaboration with Sr Director, Clinical Data Management, provide support to clinical study ...

next page

Showing results 1-20

All JobsStatistical Programmer JobsSenior Statistical Programmer JobsSenior Statistical Programmer Jobs in Berkeley, CA

Senior Statistical Programmer information

See Berkeley, CA salary details

$101K

$157.1K

$205.1K

How much do senior statistical programmer jobs pay per year?

As of Aug 1, 2026, the average yearly pay for senior statistical programmer in Berkeley, CA is $157,088.00, according to ZipRecruiter salary data. Most workers in this role earn between $131,000.00 and $181,200.00 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 popular job titles related to Senior Statistical Programmer jobs in Berkeley, CA? For Senior Statistical Programmer jobs in Berkeley, CA, the most frequently searched job titles are:
What job categories do people searching Senior Statistical Programmer jobs in Berkeley, CA look for? The top searched job categories for Senior Statistical Programmer jobs in Berkeley, CA are:
What cities near Berkeley, CA are hiring for Senior Statistical Programmer jobs? Cities near Berkeley, CA with the most Senior Statistical Programmer job openings:
Senior Statistical Programmer jobs near you
Infographic showing various Senior Statistical Programmer job openings in Berkeley, CA as of July 2026, with employment types broken down into 84% Full Time, 7% Part Time, 1% Temporary, 6% Contract, 1% Nights, and 1% Summer. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $157,088 per year, or $75.5 per hour.

Senior Manager, Statistical Programming

Kardigan

South San Francisco, CA

Other

Re-posted 7 days ago

Job description

Position Title: Senior Manager, Statistical Programming

Department: Clinical Data Sciences & Analytics 

Reports To: Head of Statistical Programming

Location: South San Francisco, CA or Princeton, NJ - On-site 4 days per week (Mon to Thurs) 

Job Overview:

The Senior Manager of Statistical Programming will be responsible for leading Statistical Programming activities. It involves hands-on implementation of statistical analyses using SAS/R, as well as performing quality reviews of deliverables, both for in-house analyses and outsourced programming tasks.

This position serves as a critical bridge between Biostatistics and Clinical Data Management (CDM), ensuring the development of CRFs and the delivery of high-quality clinical data. Additionally, this position will play an important role in helping establish SOPs and programming standards and also build our SCE platform.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Key Project Responsibilities:

  • Provides programming leadership and oversee study to compound-level programming deliverable in collaboration with the Stats lead and cross-functional teams.
  • Serve as the lead programmer to reviews SAP, Data Presentation Plan, Table Shell to align with project objectives and ensures clarity and completeness of programming assumptions and requirements.
  • Lead programming team to produce and/or validate SDTM, ADaM and TLF, for CSR and regulatory requests, publication needs, and ad-hoc analyses.
  • Manage CROs and contractors, ensuring compliance, quality of deliverables, timelines, and budget adherence.
  • Collaborate with biostatisticians and clinical development colleagues to develop/review TLF shells, SDTM, and ADaM specifications.
  • Work closely with Data Management and Biostatistics teams to ensure the accuracy of final databases, analyses, and reports.
  • Develop global tools, such as macros or graphical user interface applications, to enhance the efficiency and capacity of the Statistical Programming team.
  • Develops robust program to create define.xml, Leads the NDA eSubmission package preparation.
  • Assist Biometric in building the statistical computing environment (SCE) platform, including designing folder structure and managing access control.

Initiative Responsibilities:

  • Under guidance from Head of Statistical Programming and Compound PL, implement innovative strategies and technologies to enhance programming processes.
  • Working with manager, establish Statistical Programming standard and deploy programming strategies, specifications and programmed analysis.
  • Proactively plan, implement, and identify issues/risks and provide remediation strategies to improve programming capability.

Qualifications and Preferred Skills

Education:

  • Master's degree in Statistics/Biostatistics, Mathematics, Computer Science, or a related field.

Experience and Skill Set:

  • Minimum of 6 years statistical programming experience in the pharmaceutical, biotech or CRO clinical trial environment.
  • Advanced SAS programming skills. Extensive Hands-on experience with SDTM, ADaM, TLF programming
  • Proficient knowledge in the implementation of CDISC standards (SDTM, ADaM) and regulatory submission requirements.
  • Good knowledge of drug development process, study design, statistical methodology, regulatory guidance, statistical concepts, and medical terminology.
  • Broad expertise in statistical programming and in developing computing strategies.
  • In-depth understanding of CDISC standards including SDTM and ADaM models and extensive experience of their implementation in clinical trials.
  • Demonstrated proficiency in using SAS/R to produce analysis datasets and TFLs.
  • Knowledge of data validation, define.xml generation using Pinnacle 21.
  • Results orientated with proven problem-solving skills and a strong interest in ongoing learning.
  • Excellent communication and collaboration skills, with the ability to work closely with cross-functional teams
  • Experience managing outsourced programming activities and overseeing deliverables from CROs and contractors.
  • Adaptable and thrives in a fast-paced, startup environment while managing multiple priorities effectively.
  • Experience with regulatory audits and inspections and IR (e.g., FDA, PMDA, NMPA, EMA) is a strong advantage.

Apply