Atorus
We are seeking a
Senior Biostatistician / Clinical Data Scientist
who combines deep statistical expertise with strong R-based visualization, storytelling, and trial design experience. The ideal candidate can bridge the gap between pharma business needs, SAP/SAS specifications, and development teams, translating complex clinical requirements into actionable workstreams. About The Role We are looking for a professional to work
full-time ,
Remote from anywhere in the U.S. Key Responsibilities Provide statistical input and guidance on trial design, estimate specification, and analysis planning. Collaborate closely with clinical teams to ensure statistical approaches align with study objectives and regulatory expectations. Develop and maintain R-based visualizations and dashboards to communicate insights and support decision-making. Translate SAPs, business requirements, and clinical objectives into Jira tickets and actionable tasks for development teams. Communicate clearly across cross-functional teams, ensuring statistical rationale and clinical context are understood by non-statisticians and developers alike. Support submissions by preparing analyses and visualizations that are compliant, reproducible, and aligned with regulatory standards. Provide mentorship to junior statisticians and data scientists. Required Qualifications Advanced degree in Biostatistics, Statistics, or related quantitative field. Extensive experience in clinical trial design, statistical analysis plans, and regulatory submissions. Strong R programming skills, including visualization, Shiny dashboards, or other interactive reporting tools. Familiarity with estimands, trial design principles, and clinical endpoints. Proven ability to communicate statistical and clinical concepts to business and development teams. Experience translating SAPs and business requirements into technical specifications or Jira tickets. Preferred / Nice-to-Have Experience with SAS and CDISC standards (SDTM/ADaM). Knowledge of trial simulation, adaptive designs, or advanced modeling approaches. Experience with Posit (RStudio) or other clinical analytics platforms. Exposure to clinical trial storytelling and creating executive-ready visual outputs. Key Skills & Attributes Strong analytical and problem-solving skills. Exceptional communication skills, able to convey complex statistical concepts clearly. Senior-level ownership: proactive, detail-oriented, and focused on delivering high-quality outputs. Collaborative mindset, able to work effectively with cross-functional clinical, regulatory, and development teams. We are an equal opportunities employer and welcome applications from all qualified candidates.
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Senior Biostatistician / Clinical Data Scientist
who combines deep statistical expertise with strong R-based visualization, storytelling, and trial design experience. The ideal candidate can bridge the gap between pharma business needs, SAP/SAS specifications, and development teams, translating complex clinical requirements into actionable workstreams. About The Role We are looking for a professional to work
full-time ,
Remote from anywhere in the U.S. Key Responsibilities Provide statistical input and guidance on trial design, estimate specification, and analysis planning. Collaborate closely with clinical teams to ensure statistical approaches align with study objectives and regulatory expectations. Develop and maintain R-based visualizations and dashboards to communicate insights and support decision-making. Translate SAPs, business requirements, and clinical objectives into Jira tickets and actionable tasks for development teams. Communicate clearly across cross-functional teams, ensuring statistical rationale and clinical context are understood by non-statisticians and developers alike. Support submissions by preparing analyses and visualizations that are compliant, reproducible, and aligned with regulatory standards. Provide mentorship to junior statisticians and data scientists. Required Qualifications Advanced degree in Biostatistics, Statistics, or related quantitative field. Extensive experience in clinical trial design, statistical analysis plans, and regulatory submissions. Strong R programming skills, including visualization, Shiny dashboards, or other interactive reporting tools. Familiarity with estimands, trial design principles, and clinical endpoints. Proven ability to communicate statistical and clinical concepts to business and development teams. Experience translating SAPs and business requirements into technical specifications or Jira tickets. Preferred / Nice-to-Have Experience with SAS and CDISC standards (SDTM/ADaM). Knowledge of trial simulation, adaptive designs, or advanced modeling approaches. Experience with Posit (RStudio) or other clinical analytics platforms. Exposure to clinical trial storytelling and creating executive-ready visual outputs. Key Skills & Attributes Strong analytical and problem-solving skills. Exceptional communication skills, able to convey complex statistical concepts clearly. Senior-level ownership: proactive, detail-oriented, and focused on delivering high-quality outputs. Collaborative mindset, able to work effectively with cross-functional clinical, regulatory, and development teams. We are an equal opportunities employer and welcome applications from all qualified candidates.
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