23 Results for

Biostatistics Jobs in California

Jobs

New!

South San Francisco, CA6 days ago

$240,000–$280,000

The Senior Director will collaborate closely with Clinical Development, Translational Medicine, Biomarker Sciences, Regulatory Affairs, Data Management, Statistical Programming, Clinical Operations, and external partners. The successful candidate will play a critical role in advancing precision medicine strategies through innovative trial methodologies, biomarker-driven development, and global regulatory engagement.

San Francisco, CA30+ days ago

They are currently seeking a highly skilled and experienced Associate Director of Biostatistics to provide leadership to develop and execute statistical strategy, design and analyses for clinical trials in all phases. Please Have: MS/MA degree in related discipline and a minimum of 9 years of related experience; or, PhD in related discipline and a minimum of 5 years of related experience; or, Experience in Oncology and study Phases I-III highly preferred.

San Francisco, CA30+ days ago

They are currently seeking a highly skilled and experienced Director of Biostatistics to provide leadership to develop and execute statistical strategy, design and analyses for clinical trials in all phases. Comprehensive and detailed knowledge of: statistical experimental designs, analyses and clinical trial requirements, particularly pertaining to Oncology trials.

Newark, CA30+ days ago

Full-time

Position Summary:The Senior SAS Programmer is responsible for applying advanced programming techniques to support the development and validation of statistical programs to be used for monitoring, analyzing, and reporting of Ardelyx’ clinical trial data for regulatory submissions and publications across multiple disease areas at Ardelyx. This position works closely with Biostatisticians, Data Managers, Clinical Trial Managers, and if necessary, Contract Research Organizations (CROs) and/or SAS programming consultants, to meet project deliverables and timelines for clinical data monitoring, analyzing, and reporting.

New!

Irvine, CA2 days ago

The Senior Statistical Programmer Contractor is expected to work independently, deliver high quality programming deliverables, and collaborate effectively with Biostatistics and Clinical Data Management. Primary ResponsibilitiesDevelop complex analysis datasets, specifications, and summary outputs (tables, listings, figures, and graphs) for inclusion in clinical study reports, regulatory submissions, and internal presentations.

Los Angeles, CA30+ days ago

$90,000–$135,000 Per Year

Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes.

Irvine, CA30+ days ago

$132,000–$186,000 Per Year

The Principal Biostatistician will represent the Biostatistics department on all aspects of the clinical development process, ranging from clinical trial designs to regulatory submissions while applying scientific rigor to statistical methods and interpretation of results and also advise on the conduct of clinical studies, database development and data quality assurance with the analysis of clinical endpoints in mind. + Collaborate with core stakeholders to provide statistical expertise in support of new product development (NPD) and/or regulatory submissions (e.g., PMA, CE Mark, PMDA) and other regulatory documents as needed.

New!

Sunnyvale, CA2 days ago

$90.37–$93 Per Hour

Responsibilities:As a key member of the Clinical Affairs department, the Senior Biostatistician (Biostatistician IV) provides advanced statistical expertise to support the design, conduct, and analysis of clinical studies, ranging from early pre-market to post-market evidence generation. Data Analysis: Utilize appropriate and robust statistical and programming methodology in the analysis of clinical trial data, including complex and advanced methods as needed, ensuring high-quality results for regulatory submissions and scientific publications.

Los Angeles, CA30+ days ago

$130,000–$145,000 Per Year

As an internal expert in biostatistics, you will provide technical leadership and biostatistical input to closely collaborate with other functional teams at Arrowhead, including Clinical Development and Operations, Regulatory, Commercial, Program Management and others. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

San Diego, CA30+ days ago

Full-time

You will work cross-functionally with teams in product development, regulatory affairs, scientific affairs, and marketing, playing a pivotal role in validating Truvian’s blood testing technology for market readiness. We are developing a fully automated benchtop system that delivers lab-accurate results from a small blood sample under 30 minutes—designed for use in retail clinics or private practice settings.

Palo Alto, CA30+ days ago

$170,000–$180,000

Bachelor’s degree in Statistics, Mathematics, Computer Science, or related field with at least 10 years of programming experience in the pharmaceutical or biotech industry; or a Master’s degree with at least 7 years of relevant experience. Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.

South San Francisco, California30+ days ago

Employee

San Diego, CA30+ days ago

Full-time

The Director will architect and scale Truvian’s clinical data ecosystem — spanning database design, data pipeline integration, clinical data quality, statistical analysis, and data visualization — to support assay validation, regulatory submissions, and real-world evidence generation. Truvian is seeking a strategic and technically adept Director, Clinical Data Management & Data Science build and lead a multidisciplinary team responsible for clinical data strategy, management, analytics, and statistical sciences.

South San Francisco, CA16 days ago

Remote

$255,000–$335,000 Per Year

Establish cross-functional relationships with leaders from key cross-functional lines including Regulatory Affairs, Clinical Operations, Commercial, Program Management, etc. and leverage those relationships to manage key project issues including but not limited to Research, Development, Commercial, Manufacturing and Competitive Intelligence. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.

Irvine, California30+ days ago

$0–$45.50 Per Hour

Modify, extend, and maintain analysis tools and workflows-primarily in Python-by leveraging existing clinical models (e.g., inventory, case management, headcount, trial enrollment, site activations/deactivations) while applying clinical trial domain knowledge. * Organize, analyze, and create reproducible analyses, reports, dashboards, and data extracts to summarize moderately complex challenges across clinical affairs projects, programs, and initiatives.

Los Angeles, California11 days ago

Position Summary: Seeking a highly experienced candidate to provide leadership and coordination for the MWCCS, a large multi-site epidemiologic study focused on the natural history of HIV/AIDS, including oversight of three clinical sites, study staff, and ongoing follow-up of participants across UCLA and collaborating institutions. Under the general supervision of the Principal Investigator, the position manages study operations, protocol compliance, data oversight, regulatory submissions, budgeting and fiscal management, and coordination with national research partners to ensure consistent implementation and integrity of study procedures.

New!

San Diego, California2 days ago

A bachelor's or graduate/higher level degree from an accredited college/university that included 16 semester hours (24 quarter hours) of biological science (with one semester in microbiology), 16 semester hours (24 quarter hours) of chemistry (with one semester in organic or biochemistry), one semester (one quarter) of mathematics, AND five years of full time acceptable clinical laboratory experience in Blood Banking, Chemistry, Hematology, microbiology, Immunology and Urinalysis/Body Fluids. A. A Bachelor's or graduate/higher level degree from a regionally accredited college/university including courses in biological science, chemistry and mathematics, AND successful completion of a Medical Laboratory Scientist/Clinical Laboratory Scientist program accredited by the National Accrediting Agency for Clinical Laboratory Sciences (NAACLS) or an accrediting body recognized by the U.S. Department of Education at the time the degree was obtained.

Los Angeles, CA30+ days ago

$120,000–$140,000 Per Year

Bachelor's degree in life sciences or technical field; At least 5 years' experience of SAS programming for clinical trials; Working knowledge of SAS, including complex data manipulation, data presentation and output deliver systems; Prior experience implementing edit checks and patient profiles on active clinical trials; and. Develop, and execute edit checks and patient profile software or programs for clinical trials; Develop and execute data listing programs used by data managers, safety surveillance, medical or clinical operations personnel; Collaborate with data management to ensure appropriate data collection and reporting.

Los Angeles, CA30+ days ago

Full-time

Work with DHS teams to support the development and implementation of a pre-release model of care under CalAIM that includes but is not limited to: eligible patient identification, ECM application submission, benefit applications, assignment to community based providers, in-reach of community based providers, care plan development, and community care coordination. Specific Deliverables Support efforts to plan and implement pre- and post-release CalAIM Enhanced Care Management (ECM) Programs for justice-involved individuals and coordinate Correctional Health Services clinical care transition efforts with community-based re-entry providers.

New!

Thousand Oaks, CA3 days ago

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Combine data and people insights to coach and guide clients on HR and business-related issues to shape and affect positive change in the organization, including strategy clarification, organization design, change management, talent development, team / organizational effectiveness and workforce planning.

Palo Alto, CA30+ days ago

The Associate Director ensures will be working on biostatistics deliverables, including study design, data analysis, data mining, epidemiology-related analyses, use of clinical trial data to inform reimbursement strategy and HTA, real world evidence, quality of life data, and interpretation, reporting, and publication of results. The Associate Director, Medical Affairs Statistical Sciences Biometrics provides technical and operational support for the design, implementation and interpretation of post approval clinical trials, programs, and disease registries.

Los Angeles, California30+ days ago

Department Summary: The UCLA Fielding School of Public Health’s Department of Biostatistics is home to a stellar team of national andinternational leaders in a wide range of cutting-edge fields, including Bayesian methods, big data, causalinference, statistical computing, data science, functional data analysis, statistical genetics, hierarchical models,HIV/AIDS, image analysis, longitudinal data analysis, multivariate data, phylogeny, spatial statistics, survivalanalysis, and optimal design. This powerhouse of expertise is dedicated to preparing critically thinking graduateswith strong, highly marketable skills through our four biostatistics degree programs: Master of Data Science inHealth (MDSH), the Biostatistics; MPH in Biostatistics; MS in Biostatistics and PhD in Biostatistics.

Novato, CA30+ days ago

Full-time

This individual will design and deploy causal inference pipelines, longitudinal and multiscale temporal models, and multimodal data integration approaches connecting omics, clinical phenotypes, and wearable-derived physiological signals. The Senior Computational Scientist will play a central role in a large funded research project focused on identifying causal drivers and mechanistic pathways underlying resilience, aging trajectories, and functional decline.

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Biostatistics Jobs in California

Sr. Director, Biostatistics ALX Oncology Inc.

Associate Director Oncology Biostatistics Penfield Search Partners

Director Biostatistics - Oncology Penfield Search Partners

Senior SAS Programmer Ardelyx

Senior Statistical Programmer Lancesoft

Statistical Programmer/Sr. Statistical Programmer Arrowhead Pharmaceuticals

Principal Biostatistician Edwards Lifesciences

Biostatistician 4 Iconma

Biostatistician (Senior Associate) Arrowhead Pharmaceuticals

Staff Biostatistician Truvian Sciences

Senior Manager, Statistical Programming - Job ID: 1646 Ascendis Pharma

Decision Analytics Associate Consultant - HEOR Evidence Generation ZS

Director, Clinical Data Management & Data Science Truvian Sciences

Medical Director, Clinical Development (Oncology) Allogene Therapeutics

Data Analytics Analyst (Onsite) Roth Staffing Companies

ACAD PRG MGT SUPV 2 The Regents of the University of California on behalf of their Los Angeles Campus

Clinical Laboratory Scientist GS-0644-11 Defense Health Agency Civilian Corps, Falls Church, VA

Manager, Clinical Programming Arrowhead Pharmaceuticals

Staff Analyst, Health Public Health Foundation Enterprises, In

Human Resources Senior Director: Human Resources Business Partner (Global Development) Amgen

Associate Director, Medical Affairs Statistical Sciences, Biometrics - ID: 1799 Ascendis Pharma

PROJECT POLICY ANL SUPV 2 The Regents of the University of California on behalf of their Los Angeles Campus

Senior Computational Scientist – Furman Lab Buck Institute

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