Penfield Search PartnersAssociate Director Oncology Biostatistics Penfield Search PartnersAssociate Director Oncology BiostatisticsSan Francisco, CAThey 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.
ALX Oncology Inc.Sr. Director, Biostatistics ALX Oncology Inc.Sr. Director, BiostatisticsSouth San Francisco, CA$240,000–$280,000The 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.
Exelixis IncExecutive Director, Biostatistics Exelixis IncExecutive Director, BiostatisticsAlameda, CAKnowledge/Skills: • Strong people management and interpersonal skills • Strong communication skills • Strong conflict management skills • Comprehensive and detailed knowledge of statistical experimental designs, analyses, and clinical trial requirements, particularly pertaining to oncology trials. EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: • MS/MA degree in Statistics/Biostatistics or related discipline and a minimum of 16 years of related experience; or, • PhD in Statistics/Biostatistics or related discipline and a minimum of 15 years of related experience; or, • Equivalent combination of education and relevant experience in oncology.
Maze Therapeutics IncDirector, Biostatistics Maze Therapeutics IncDirector, BiostatisticsSouth San Francisco, CA$228,000–$280,000 / yearThe company is advancing a pipeline using its Compass platform, which allows it to identify and characterize genetic variants in disease and then link those variants to the biological pathways that drive disease in specific patient groups through a process it refers to as variant functionalization. Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing the power of human genetics to develop novel, small molecule precision medicines for patients living with renal, cardiovascular and related metabolic diseases, including obesity.
Penfield Search PartnersDirector Biostatistics - Oncology Penfield Search PartnersDirector Biostatistics - OncologySan Francisco, CAThey 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.
Exelixis IncBiostatistics Director Exelixis IncBiostatistics Directoralameda, CA$187,500–$266,000 / yearEDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: BS/BA degree in Statistics/Biostatistics or related discipline and a minimum of thirteen years of related experience; or, MS/MA degree in Statistics/Biostatistics or related discipline and a minimum of eleven years of related experience; or, PhD in Statistics/Biostatistics or related discipline and a minimum of eight years of related experience, or; Equivalent combination of education and experience. Knowledge/Skills: Comprehensive and detailed knowledge of: statistical experimental designs, analyses and clinical trial requirements, particularly pertaining to oncology trials.
eTeam Inc.NewBiostatistician 4 eTeam Inc.Biostatistician 4Sunnyvale, CA$80–$85 / hourAs 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.
ZSDecision Analytics Associate Consultant - HEOR Evidence Generation ZSDecision Analytics Associate Consultant - HEOR Evidence GenerationSouth San Francisco, California
Allogene TherapeuticsNewMedical Director, Clinical Development (Oncology) Allogene TherapeuticsMedical Director, Clinical Development (Oncology)South San Francisco, CARemote$255,000–$335,000 / yearEstablish 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.
Intuitive Surgical IncVP of Global Clinical Affairs Intuitive Surgical IncVP of Global Clinical AffairsSunnyvale, CACore competencies of this position include: Expert knowledge and understanding of all clinical specialties and technology platforms that Intuitive serves; Significant experience and proven success leading multiple teams in the medical device or related industry; Significant experience leading clinical affairs strategies and objectives; Ability to create departmental vision, strategy, and strategic objectives and guide teams in their execution; Establish effective programs, guidelines, and procedures for global clinical affairs activities. This leader will help support regulatory submissions and the generation of high-impact clinical evidence through publications, presentations, abstracts, and scientific collaborations that enable market access, adoption, and reimbursement worldwide.
Karwell TechnologiesStatistician Karwell TechnologiesStatisticianSan Francisco, CAProvides general infrastructure support to the Department (presents / teaches at the department meetings, contributes to other general department documents or policies, assists with newsletter, helps in department libraries, or trains new hires). Supports the department by directly contributing to simple or moderately complex study protocols and bid defenses, including organizing teams and implementing strategies to ensure process and programming efficiencies.
Katalyst Healthcares & Life SciencesStatistician Katalyst Healthcares & Life SciencesStatisticianSan Francisco, CAProvides general infrastructure support to the Department (presents / teaches at the department meetings, contributes to other general department documents or policies, assists with newsletter, helps in department libraries, or trains new hires). Supports the department by directly contributing to simple or moderately complex study protocols and bid defenses, including organizing teams and implementing strategies to ensure process and programming efficiencies.
The Fountain Group LLCSr. Analyst - III* The Fountain Group LLCSr. Analyst - III*Tampa, CARemotePhD, MD, ScD, PharmD, or related doctoral degree in Epidemiology, Outcomes Research, Biostatistics, Medicine, or similar field with 8+ years of relevant experience; OR Master’s degree with 10+ years of relevant experience. Strong expertise in observational study design, causal inference, real-world data sources (claims, EHR, registries), bias/confounding, and sensitivity analyses.
Ascendis PharmaSenior Manager, Statistical Programming - Job ID: 1646 Ascendis PharmaSenior Manager, Statistical Programming - Job ID: 1646Palo Alto, CA$170,000–$180,000Bachelor’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.
Net2SourceSr. Analyst - Real World Evidence (RWE) Net2SourceSr. Analyst - Real World Evidence (RWE)Foster City, CARemote$100–$113.75 / hourAs Contractor, Real-World Evidence, you will provide strategic, scientific, and operational support for real-world evidence generation across the product lifecycle, with a core focus on the design and execution of external control arms (ECAs) and other complex observational studies. " Provide end to end support for RWE studies, including, study design, protocol and SAP development, data source selection and feasibility, vendor oversight and quality control, analysis, interpretation, reporting, and financial stewardship.
Integrated Resources, IncSr. Analyst - III Integrated Resources, IncSr. Analyst - IIIFoster City, CA$110–$115.41 / hourJob Description: As Contractor, Real-World Evidence, you will provide strategic, scientific, and operational support for real-world evidence generation across the product lifecycle, with a core focus on the design and execution of external control arms (ECAs) and other complex observational studies. " Provide end to end support for RWE studies, including, study design, protocol and SAP development, data source selection and feasibility, vendor oversight and quality control, analysis, interpretation, reporting, and financial stewardship.
MindlanceSr. Analyst - III* MindlanceSr. Analyst - III*Foster City, CA$95.83–$102.01 / hourJob Description: As Contractor, Real-World Evidence, you will provide strategic, scientific, and operational support for real-world evidence generation across the product lifecycle, with a core focus on the design and execution of external control arms (ECAs) and other complex observational studies. " Provide end to end support for RWE studies, including, study design, protocol and SAP development, data source selection and feasibility, vendor oversight and quality control, analysis, interpretation, reporting, and financial stewardship.
MindlanceSenior Manager - Medical Affairs* MindlanceSenior Manager - Medical Affairs*Foster City, CA$72.72–$77.42 / hourJob Description: The RWE Analyst will contribute to the Kite Real-World Evidence/Health Economic Outcomes Research (RWE/HEOR) Team as part of an effort to contribute to the strategies of the broader Kite Evidence Generation Team, which will include the conduct of timely, relevant, and rigorous analysis of real-world data (RWD) to address critical research questions and contribute to cross-functional initiatives. The RWE Analyst will be responsible for developing, reviewing, and providing feedback on study documents, such as protocols and statistical analysis plans, and executing planned data analyses using administrative claims, electronic health record (EHR), and observational registry databases.
Abbott LaboratoriesSenior Biostatistician Abbott LaboratoriesSenior BiostatisticianSanta Clara, CAIf you provide content to customers through CloudFront, you can find steps to troubleshoot and help prevent this error by reviewing the CloudFront documentation. CloudFront Request ID: Ol4MigTQ0BwYwDXKLHrE9YdApDN7fDwysllCBs_vzjhWOqkMcg8YIQ.
Abbott LaboratoriesAssociate Biostatistician Abbott LaboratoriesAssociate BiostatisticianSanta Clara, CAIf you provide content to customers through CloudFront, you can find steps to troubleshoot and help prevent this error by reviewing the CloudFront documentation. Generated by cloudfront CloudFront Request ID: l_tium43UNhgSjvcOYJIUZgTZZhHk779NxrLlWQAkenKzmbACRDPUg.
Ascendis PharmaAssociate Director, Medical Affairs Statistical Sciences, Biometrics - ID: 1799 Ascendis PharmaAssociate Director, Medical Affairs Statistical Sciences, Biometrics - ID: 1799Palo Alto, CAThe 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.