Statistician Salary at Ucsf Health BETA

Our client is a biopharmaceutical company with marketed product, a robust pipeline and solid financials, focused in the Rare Disease area. They are currently seeking a Director or Senior Director of Biostatistics (depending on experience) to be responsible for statistical activities supporting clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data. This is a hands-on role where you will interact with internal and external cross-functional study teams, support interactions with Health Authorities globally, and manage CRO programmers and statisticians in preparing analysis files and performing statistical analyses. Lead statistical and statistical programming team on product level Provide statistical input to strategic planning, study design, protocol development, sample size calculation, CRF, Results Interpretation, clinical study repor

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: The Associate Director in CMC Statistics is responsible for providing statistical support across a broad range in nonclinical areas with a focus on Chemistry, Manufacture and Control (CMC), expanding and broadening the application of Biostatistics. He/she is also responsible for helping the group head build the group infrastructure (e.g., developing SOPs) and mentor junior statisticians or interns. Responsibilities: * Apply statistical techniques to facil

ROLE SUMMARY * Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices. * Provide scientifically rigorous statistical expertise on: Projects and protocols in support of clinical development and for publication, presentation, access negotiation, and other evidence generation efforts for Pfizer products; Regulatory and Health Technology Assessment (HTA) submissions; and projects to maximize the value of aggregate clinical and real world data in support of drug development and other scientific strategies. * Provide study and other project level statistical counsel and communicate resource needs to teams. ROLE RESPONSIBILITIES * Provide scientifically rigorous statistical expertise on study design, statistical analysis plans, interpretation and communication of statistical results, project development plans, regulatory issues, and scientific and other product support projects. * Pr

POSITION SUMMARY: The Senior Research Associate 1 performs research and/or development tasks in collaboration with others. Makes detailed observations, analyzes data, and interprets results. Investigates, creates and develops new methods and technologies for project advancement. Maintains a high level of professional expertise through familiarity with scientific literature. PRIMARY RESPONSIBILITIES: Design, plan, and perform experiments geared towards the development of non-invasive cancer detection and cancer monitoring tests. Autonomously and accurately plan and execute complex laboratory experiments Analyze data using advanced analytical tools Keep detailed laboratory notes in electronic format; write protocols and experimental plans, and document results and scientific interpretations Contribute insight toward experimental findings and troubleshoot laboratory processes and protocols Communicate and discuss results with a multidisciplinary team including biologists, bioinformatician

POSITION SUMMARY: We are looking for an inquisitive and creative Staff Scientist to be a key member of our Molecular Biology Research Team. As a successful candidate, you will work on initiating, directing and executing pre-product scientific research to build tools & technology to expand Natera's state-of-the-art product portfolio. Candidates with deep understanding of molecular biology and significant experience in developing NGS oncology assay for MRD detection will be considered. PRIMARY RESPONSIBILITIES: Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problem solving Independently leads projects to create and develop novel nucleic acid based diagnostic tests; including planning, feasibility testing, protocol development, and optimization Responsible for executing projects as per associated timelines and deliverables Ability to work cross functionally with other groups such as statistics and bioinfo

POSITION LOCATION: Position is available as a hybrid position in San Carlos, Bay Area, California as well as a remote position (within US). POSITION SUMMARY: Natera is currently seeking a Lead/Staff Bioinformatics Scientist to join our Bioinformatics Research Team focused on Epigenomics in Oncology. Natera's mission is to change the management of disease worldwide by using information gained from a simple blood draw to detect disease early and proactively inform treatment. The ideal candidate should have a strong background in algorithm development, genomics, sequencing data processing, and/or applied machine learning. The individual will serve as a technical lead for various algorithm and machine learning model development projects. RESPONSIBILITIES: Design, implement, and validate innovative algorithms and statistical methods to analyze large-scale data sets related to cancer detection Foster a culture of innovation, collaboration, and scientific excellence Work closely with molecula

Waymo is an autonomous driving technology company with the mission to be the most trusted driver. Since its start as the Google Self-Driving Car Project in 2009, Waymo has focused on building the Waymo Driver-The World's Most Experienced Driver™-to improve access to mobility while saving thousands of lives now lost to traffic crashes. The Waymo Driver powers Waymo One, a fully autonomous ride-hailing service, and can also be applied to a range of vehicle platforms and product use cases. The Waymo Driver has provided over one million rider-only trips, enabled by its experience autonomously driving tens of millions of miles on public roads and tens of billions in simulation across 13+ U.S. states. The Planner Evaluation team works on one of the key challenges in autonomous driving: measuring and improving the quality of the software that drives the car. We are looking for experienced software engineers and data scientists to help us understand and improve the performance of Waymo's ML an

Are you passionate about leading and supporting statistical programming activities to support drug development? Do you have experience within SAS and CDISC standards, project and resource management? If so, you have the chance to join Ascendis Pharma as our new Associate Director, Statistical Programming. Ascendis Pharma is a fast-growing, dynamic biopharmaceutical company with Headquarters in Denmark that offers you room to grow and the freedom to take responsibility and make a difference for patients every day. As a member of our global team, you will work with highly skilled and passionate colleagues to advance our exciting product pipeline. The Role As our new Senior Manager or Associate Director, Statistical Programming (level commenserate with experience), you will manage internal and external resources to lead, or support assigned project statistical programming activities. You will provide programming support to statisticians in production of summary tables, data listings and g