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Manager Statistical Programming Jobs in California

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Manager Statistical Programming information

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$83.4K

$145.4K

$245.7K

How much do manager statistical programming jobs pay per year?

As of Aug 19, 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?

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:

Infographic showing various Manager Statistical Programming job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Remote job distribution, with an average salary of $145,363 per year, or $69.9 per hour.

Senior Analyst, Statistical Programming

Edwards Lifesciences Belgium

Irvine, CA โ€ข On-site

$119 - $168/hr

Other

Posted yesterday

New


Job description

Dedicated to innovation, our Surgical business unit is focused on identifying and solving critical, unmet needs in cardiac surgery. In understanding the challenges of open-heart surgery, we partner with surgical teams to deliver modern technologies intended to enhance patientsโ€™ quality of life and expand their potential treatment opportunities. Itโ€™s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

How youโ€™ll make an impact:
  • Plan the execution of programs in statistical programming languages within project.

  • Develop complex analysis datasets, specifications, and summary output (tables, listings, or graphs) for inclusion in clinical reports or presentations; Create complex programs that meet regulatory and company standards to permit efficient programming, reporting, and review, utilizing statistical programming languages (e.g SAS)

  • Review and validate statistical programs and ensure that all appropriate program validation documentation to meet regulatory and company standards are consistently structured to permit efficient programming, reporting, and review

  • Perform complex analysis in response to data requests in collaboration with designated statistician

  • Collaborate with CDM (Clinical Data Management) and designated statistician to review draft CRFs (Case Report Forms), database specifications, and perform edit checks

  • This role is an on-site position at our Edwards Life sciences corporate headquarters in Irvine, California

What you'll need (Required):
  • Bachelor's Degree in Statistics, Mathematics, Computer Science or related field , 4 years experience previous statistical programming experience (e.g. SAS)

  • Master's Degree or equivalent in Statistics, Mathematics, Computer Science or related field , 2 years experience previous statistical programming experience (e.g. SAS)

  • This role is an on-site position at our Edwards Life sciences corporate headquarters in Irvine, California

What else we look for (Preferred):
  • Skills of leveraging emerging AI and automation capabilities to enhance efficiency, quality, and scalability of statistical programming workflows.

  • Proven expertise in interfacing MS Office Suite with SAS

  • Good written and verbal communication skills and interpersonal relationship skills including consultative and relationship management skills

  • Full understanding and knowledge relevant to statistical programmingFull understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device settingStrong problem-solving, organizational, analytical and critical thinking skills

  • Experience working in clinical trials within a pharmaceutical/medical device industry

  • Good leadership skills and ability to influence change

  • Strict attention to detail

  • Ability to interact professionally with all organizational levels

  • Ability to manage competing priorities in a fast paced environment

  • Must be able to work in a team environment, including inter-departmental teams and key contact representing the organization on projects

  • Ability to interact with senior internal and external personnel on significant matters often requiring coordination between organizations

  • Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For California, the base pay range for this position is $119,000 - $168,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

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