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Manager Statistical Programming Jobs in California

Erasca

SVP Biometrics

San Diego, CA

This includes leadership of the Biostatistics, Statistical Programming & Analysis, and Clinical Data Management functions. This role requires hands-on execution as well as oversight of internal and ...

Erasca

SVP Biometrics

San Diego, CA · On-site

This includes leadership of the Biostatistics, Statistical Programming & Analysis, and Clinical Data Management functions. This role requires hands-on execution as well as oversight of internal and ...

Erasca

SVP Biometrics

San Francisco, CA · On-site

This includes leadership of the Biostatistics, Statistical Programming & Analysis, and Clinical Data Management functions. This role requires hands-on execution as well as oversight of internal and ...

Erasca

SVP Biometrics

San Diego, CA · On-site +1

This includes leadership of the Biostatistics, Statistical Programming & Analysis, and Clinical Data Management functions. This role requires hands-on execution as well as oversight of internal and ...

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All JobsStatistical Programming JobsManager Statistical Programming JobsManager Statistical Programming Jobs in California

Manager Statistical Programming information

See California salary details

$83.4K

$145.4K

$245.7K

How much do manager statistical programming jobs pay per year?

As of Jul 9, 2026, the average yearly pay for manager statistical programming in California is $145,363.00, according to ZipRecruiter salary data. Most workers in this role earn between $123,400.00 and $157,900.00 per year, depending on experience, location, and employer.

What is a Manager Statistical Programming job?

A Manager Statistical Programming oversees a team of statistical programmers who support clinical trials and research by developing, validating, and maintaining statistical programs. They ensure compliance with regulatory requirements, manage project timelines, and collaborate with statisticians, data managers, and other stakeholders. This role requires strong programming skills in SAS or other statistical software, leadership abilities, and expertise in clinical data standards such as CDISC.

What are the typical daily responsibilities of a Manager Statistical Programming?

As a Manager Statistical Programming, your daily responsibilities usually include overseeing a team of statistical programmers, coordinating the development and validation of statistical programs for clinical trial data analysis, and ensuring deliverables meet regulatory and company quality standards. You will often interact with biostatisticians, data managers, and clinical teams to align programming outputs with study goals. Additionally, you may review project timelines, allocate resources, mentor junior programmers, and contribute to process improvement initiatives. This multifaceted role requires balancing technical oversight with leadership and interdepartmental communication.

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

To excel as a Manager Statistical Programming, you need a solid background in statistics, programming (such as SAS, R, or Python), and experience with clinical trial data management, often supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory guidelines (e.g., FDA, ICH), data standards such as CDISC, and certifications in relevant programming languages or clinical data processes are highly beneficial. Strong leadership, project management, and effective communication skills are essential for guiding teams and collaborating with cross-functional departments. These skills enable the manager to deliver high-quality statistical programming deliverables, ensure regulatory compliance, and drive team performance in a deadline-driven environment.

What are the most commonly searched types of Statistical Programming jobs in California? The most popular types of Statistical Programming jobs in California are:
What are popular job titles related to Manager Statistical Programming jobs in California? For Manager Statistical Programming jobs in California, the most frequently searched job titles are:
What job categories do people searching Manager Statistical Programming jobs in California look for? The top searched job categories for Manager Statistical Programming jobs in California are:
What cities in California are hiring for Manager Statistical Programming jobs? Cities in California with the most Manager Statistical Programming job openings:
Manager Statistical Programming jobs near you
Sr. Statistical Programmer

Sr. Statistical Programmer

Kodiak Sciences Inc.

Palo Alto, CA • On-site

Full-time

Posted 15 days ago

Job description

Kodiak Sciences Inc. is a rapidly growing, clinical-stage biopharmaceutical company dedicated to transforming ophthalmology through innovative therapeutics. Our proprietary Antibody Biopolymer Conjugate Drug (ABCD) platform integrates protein engineering, polymer chemistry, small molecule drug discovery, and advanced drug delivery technologies to address prevalent and debilitating retinal diseases with the goal of improving patient outcomes worldwide. In this fast-growing and fast-paced organization, your expertise is needed to provide support for clinical and statistical programming activities related to multiple clinical studies.

Key Responsibilities

  • Assist in the review of key study-related documents produced by other functions, e.g. Statistical Analysis Plan, Case Report Forms, Data Management Plan, Database Specifications, EDC Data Structures, DMC plans and other clinical documents
  • Write, test and validate SAS programs to produce analysis datasets, TLFs, to be included in reports for submission to regulatory agencies, publications and other communications as needed
  • May serve as a technical lead and project manager for multiple studies managing all aspects of study deliverables related to statistical and clinical programming as needed
  • Work with internal stakeholders to gather requirements and write specifications
  • Interact and communicate with Statisticians, Data Managers, Clinical Operations, Medical Monitors, Medical Writing and Medical Monitors to address programming related study deliverables
  • Write macros for reusability
  • Review and verify vendor deliverables for quality and accuracy
  • Contribute to the development review of Statistical Programming policies, standard operating procedures and other controlled documents
  • Interface with outsourcing partners and vendors

Education & Experience

  • B.S. preferably in Mathematics, statistics, computer sciences or other related field
  • 5+ years of clinical trials experience in pharmaceutical or biopharmaceutical setting or equivalent

Additional Skills

  • Thorough knowledge of the drug development and regulatory submission cycle
  • Excellent project management skills
  • Excellent communication skills
  • Able to work in a fast pace and agile environment
  • In-depth and current knowledge of regulatory requirements and guidance
  • Excellent SAS and CDISC skills
  • Proficiency in MS Word, Excel, PowerPoint, and Project

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