Principal Biostatistician Biogen IncPrincipal BiostatisticianCA$134,000–$179,000 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. Your ability to effectively communicate complex statistical concepts in lay terms sets you apart, alongside your leadership skills and ability to work collaboratively with diverse teams.
Senior Principal Biostatistician - West Coast Hub Biogen IncSenior Principal Biostatistician - West Coast HubCA$127,000–$156,000 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. Biogen's West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster.
Biostatistician I University of Southern CaliforniaBiostatistician ILos Angeles, CAResponsibilities include preparing and analyzing complex longitudinal and spatial datasets, under the direction of principal investigators, developing analytic strategies aligned with study aims, translating findings into actionable scientific outputs, and developing charts and graphs to display results; may assist in writing research papers for publication, presentations, or preparing statistical reports for management. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.
Senior Biostatistician University of Southern CaliforniaSenior BiostatisticianLos Angeles, CA$140,000–$190,000 / yearOur academic programs are augmented by numerous research centers, institutes and initiatives that provide additional research expertise and experiences, notable among them are: The Judith and John Bedrosian Center on Governance and the Public; The Center for Philanthropy and Public Policy; The USC Lusk Center for Real Estate; The METRANS Transportation Consortium; The Leonard D. Schaeffer Center for Health Policy & Economics; and The Schwarzenegger Institute for State and Global Policy. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal salary data, federal, state and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.
Senior Staff Biostatistician N-Power Medicine IncSenior Staff BiostatisticianCARemote$186,000–$259,000 / yearCollaborates with Clinical Science and Commercial teams to provide statistical leadership for innovative clinical development projects, including providing strategic input into clinical study plans and protocols, regulatory strategy, target product profiles (TPPs), and integrated evidence plans. This responsibility includes working in close collaboration with other QS experts, Clinical Science Product Data Abstractors, and other cross-functional partners to conduct next generation external control arms ECAs that integrate retrospective and prospective real-world data with single arm and randomized clinical trials.
Principal Biostatistician Edwards LifesciencesPrincipal BiostatisticianIrvine, CA$132,000–$186,000 / yearThe 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.