Biostatistician Research Scientist collaborating with faculty and investigators on study design, data management, programming, analysis, and dissemination of research findings.
Compensation
$78,000 to $90,000
Responsibilities
Collaborate on research design and sample size determination
Oversee data management and integration
Implement and optimize statistical programming using R and Python
Create data visualizations and contribute to publications
Provide design and analysis support and mentor junior researchers
Requirements
Graduate level training in Biostatistics, Statistics, or Data Science
Nice to have: data management and integration
Nice to have: experience with NIH/NIDDK consortia
Nice to have: experience with multiple NIH funded cohorts
Nice to have: proficiency in several statistical programming software languages
Developing and validating R programs for statistical analysis and reporting of clinical trial data.
Leading more than one Statistical Programming team to create, validate and generate statistical outputs, including listings, tables, figures, and CDISC-compliant SDTM and ADaM datasets.
Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data.
Performing quality control and validation of statistical outputs, ensuring accuracy, consistency, and regulatory compliance.
Assisting in the preparation of statistical reports, presentations, and publications to support regulatory submissions and clinical study reporting.
Requirements
Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related quantitative field.
Provide statistical support for assigned clinical studies under the guidance of the Biometrics/Biostatistics Team Lead or other senior statistical leadership.
Compensation
Target Base Pay Range: $116,000.00 - $151,000.00
Responsibilities
Provide statistical support for assigned clinical studies under the guidance of the Biometrics/Biostatistics Team Lead or other senior statistical leadership.
Collaborate with clinical, data management, statistical programming, and other cross-functional team members to support study activities.
Contribute statistical input to study design, protocol development, endpoint definition, and analysis planning.
Prepare and review assigned statistical analysis plans, case report forms, clinical database specifications, validation plans, table, figure, and listing shells, analysis dataset specifications, and related documentation.
Perform statistical analyses, simulations, and ad hoc analyses as needed.
Requirements
Master's degree in Statistics, Biostatistics, or related field
Ph.D. preferred
Nice to have: R or other statistical software
Nice to have: experience with external vendors or contract research organizations
Highly experienced technical leader providing strategic leadership in clinical and statistical programming focusing on AI, automation, and innovative methodology to improve portfolio efficiency and quality.
Locations (3)
Raritan, New Jersey, United States
Spring House, Pennsylvania, United States
Titusville, New Jersey, United States
Compensation
$140,000.00 - $241,500.00
Responsibilities
Provide strategic technical leadership and expertise in Clinical and Statistical Programming
Drive AI readiness and adoption by defining use cases and success measures
Identify and implement strategic opportunities for innovative new tools and technologies
Lead complex departmental innovation and process improvement projects
Lead biostatistician overseeing complex clinical trial studies, managing statistical strategy, design, analysis, and regulatory submissions.
Responsibilities
Serve as lead statistician on complex key client studies
Act as point-of-contact ensuring cohesive communication with sponsors and internal teams
Lead project-level statistical strategy from protocol/SAP planning through reporting
Develop sample size estimation, modeling approaches, adaptive or Bayesian frameworks, and innovative trial designs
Provide senior oversight for statistical deliverables including SAPs, randomization specifications, and statistical contributions to CSRs, publications, and regulatory documents
Requirements
Advanced degree (MS or PhD) in statistics or closely related field
Lead and execute complex data analyses, build data pipelines, ensure data quality, manage projects, supervise staff, and translate data into actionable insights for health policy research.
Locations (2)
Los Angeles, California, United States
Washington, District of Columbia, United States
Compensation
The annual base salary range for this position is $105,664.88 - $122,141.8.
Responsibilities
Lead and execute complex data analyses using large-scale health care data
Design and build data pipelines, research tools, and analytic infrastructure
Ensure data quality and reproducibility through rigorous quality assurance processes
Manage projects, including timelines, deliverables, and coordination with cross-functional team members
Supervise and mentor junior staff
Requirements
MA/MS in statistics, data science, economics, applied mathematics, or related quantitative field (or equivalent combined education and work experience)
Lead Clinical Data Management and Statistical Programming functions within Clinical Affairs, overseeing data acquisition, analysis, and delivery for global regulatory submissions.
Compensation
The annualized base salary range for this hourly role is $124,200 to $206,800 and is bonus eligible.
Responsibilities
Provide strategic and operational leadership for Clinical Data Management and Statistical Programming
Recruit, develop, and retain high-performing teams
Establish goals, performance metrics, and operating processes
Manage budgets, priorities, and resources across multiple studies
Partner with senior leadership and cross-functional stakeholders
Requirements
Bachelor's degree in Life Sciences, Computer Science, Statistics, Data Science, Information Systems
Master's degree in related field
Nice to have: Experience with AI-enabled tools in clinical data management
Nice to have: Experience in diagnostics, in vitro diagnostics, medical devices
Nice to have: Experience leading selection, implementation, validation of clinical technology platforms
The Senior Manager, C&SP Methodology is a highly experienced technical and team leader with an in-depth understanding of clinical and/or statistical programming processes, tools/systems and strong project and team leadership skills. This position is accountable for influencing, shaping and developing technical and process strategy and solutions that deliver increased quality, efficiency, and innovation solutions within the functional area.
Locations (3)
Raritan, New Jersey, United States
Spring House, Pennsylvania, United States
Titusville, New Jersey, United States
Compensation
The anticipated base range for this position is $140,000.00 - $241,500.00
Responsibilities
Providing strategic technical leadership and expertise in roles that directly support Clinical and Statistical Programming Therapeutic Area / assigned group, research and innovation in emerging spaces, including AI, and/or standard tools development.
Strategic partnering with leads, user community and departmental/external stakeholders to identify innovation, automation and continuous improvement opportunities.
Proposes, evaluates and develops solutions and strategies that drive competitive advantage.
Applying a strong customer focus to evaluate stakeholder needs/requirements, thinking broadly end-to-end and deliver relevant solutions, in alignment with departmental technical strategies.
Leading complex departmental innovation and process improvement projects.
Biostatistician - Research ScientistNewUniversity of Colorado · Aurora, US
Manager, Clinical Data and SystemsHologic Careers · San Diego, US