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Full Time Statistical Programmer Jobs in California

AEG Worldwide

LA Kings - Sr. Data Analyst

El Segundo, CA · On-site

$91K - $115K/yr

Expertise in SQL, statistical programming (Python) and Spark * Experience working with MLOps ... Benefits Full-time: We offer a comprehensive benefits package that includes: medical, dental and ...

RZR Global Inc.

Analyst- SF

San Francisco, CA · On-site

$85K - $150K/yr

Graduate of Mathematics, Statistics, Engineering, Computer Science, or any other analytical field ... The San Francisco salary range for this full-time position is $85,000-$150,000 inclusive of base ...

Luster National

Reporting Data Scientist

Sacramento, CA · On-site

This is a long-term, full-time, on-site position located in Sacramento, CA. Responsibilities may ... Master's degree in data science, computer science, statistics, engineering, business analytics, or ...

Agilent

Validation Engineer

Carpinteria, CA · On-site

$88K - $137K/yr

Reports into the Manufacturing engineering function. The Carpinteria site manufactures cancer ... statistics-based approach to validation. Additional Details This job has a full time weekly ...

Workato

Staff Analytics Engineer

Palo Alto, CA · On-site

Full-time telecommuting is an option. Minimum Requirements: Bachelor's degree (or its foreign ... Statistics, Engineering (any field), or a related quantitative discipline, and two (2) years of ...

Workato

Staff Analytics Engineer

Palo Alto, CA · On-site +1

Full-time telecommuting is an option. Minimum Requirements: Bachelor's degree (or its foreign ... Statistics, Engineering (any field), or a related quantitative discipline, and two (2) years of ...

search-tactics

Product Engineer

Cudahy, CA · On-site

Direct Hire/Full Time Salary: $100K - $150K DOE One of Client is currently looking for a Product ... Knowledge and application of statistics. Occasionally, we take a leadership role in resolving cross ...

Peak Energy

Staff Reliability Engineer

Burlingame, CA

$115K - $145K/yr

Staff Reliability Engineer Position Type: Full-time About Peak Energy Peak Energy is the first ... Proficiency using statistical analysis tools in Python or equivalent for modeling and data analysis

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Full Time Statistical Programmer information

What is the difference between Full Time Statistical Programmer vs Clinical Data Analyst?

AspectFull Time Statistical ProgrammerClinical Data Analyst
Required CredentialsBachelor's or Master’s in Statistics, Biostatistics, or related field; programming skills in SAS, R, or PythonBachelor's or Master’s in Statistics, Data Science, or related; strong analytical and programming skills
Work EnvironmentPharmaceutical or biotech companies, CROs, clinical research settingsHealthcare organizations, research institutions, pharmaceutical companies
Employer & Industry UsageCommonly employed in clinical trials to generate statistical reportsFocuses on data interpretation, reporting, and supporting clinical decision-making

The main difference is that Full Time Statistical Programmers primarily develop and validate statistical programs for clinical trials, while Clinical Data Analysts focus on analyzing and interpreting clinical data to support research and decision-making. Both roles require strong programming skills and work in similar environments, but their core responsibilities differ.

What are the most commonly searched types of Statistical Programmer jobs in California? The most popular types of Statistical Programmer jobs in California are:
What cities in California are hiring for Full Time Statistical Programmer jobs? Cities in California with the most Full Time Statistical Programmer job openings:
Full Time Statistical Programmer jobs near you
Director, Biostatistics - Early Phase

Director, Biostatistics - Early Phase

Revolution Medicines

Redwood City, CA • On-site

Full-time

Posted 19 days ago

Job description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
Playing a critical role as a lead statistician for clinical program(s) and studies and the subject matter expert (SME) in Biostatistics within Quantitative Sciences function, this position is to provide statistical leadership and support for clinical development strategy and clinical studies through product life cycle.
  • Provide statistical support and strategic input to clinical development plans and target product profiles, proof of concept criteria, and team's preparation for company governance reviews.
  • Represent Biostatistics function on cross-function teams at program level and serve as a lead statistician for oncology studies
  • Collaborate with various functions on study design and planning, protocol development, statistical analysis plan and analysis specifications.
  • Provide statistical support for study protocol development, analysis plan and specification through direct involvement and/or providing guidance to junior staff.
  • Plan and prepare independent data monitoring committee (DMC), coordinate with independent statistical data analysis center for DMC and study team for periodic DMC reviews.
  • Collaborate with data management and clinical operations over the course of clinical studies to provide statistical input to study conducts and database development as well as data collection and cleaning activities.
  • Collaborate with statistical programming to ensure that appropriate programs and documentations are being developed for datasets development and outputs generation, and ensure the statistical analyses specified in scientific protocols and/or analysis plans are conducted appropriately.
  • Provide statistical input and leadership to the development of global health authority documents, regulatory interaction and response to health authority submissions.
  • Provide statistical support for clinical publications, assist in data interpretation to ensure consistency and accuracy in data presentation.
  • Drive and lead department initiatives, best practices, and guidelines.
  • Keep abreast in new developments in statistics, drug development, and regulatory guidance and share knowledge with functional and cross-functional team members.

Required Skills, Experience and Education:
  • D. or M.S. in Statistics/Biostatistics, a minimum of 8 years (for Ph.D.) and 12 years (for M.S.) of experience in the biotech/pharma industry as a statistician. Level will be determined based on the relevance of experience.
  • Hands-on experience in design and analysis of oncology trials is a must.
  • Ability to work independently and within a team.
  • Solid knowledge in ICH and other regulatory requirements related to biostatistical activities and clinical trials.
  • Excellent verbal and written communication skills are required.
  • Good interpersonal and project management skills are essential.
  • Proficiency in SAS and/or R.

Preferred Skills:
  • Active participation in NDA/BLA filing through label negotiations desirable. #LI-Hybrid #LI-SH1

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
Base Pay Salary Range
$211,000-$264,000 USD
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.
If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.

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