The Principal Statistical Programmer will independently manage clinical trial reporting activities, including generating SDTM and ADaM datasets and complex statistical outputs. They will also oversee CRO programming deliverables to ensure high-quality, consistent data summaries that meet regulatory and project timelines.
The role involves preparing programming scripts to generate NONMEM analysis datasets and managing e-submission packages for PK/PD modeling. You will also provide guidance to junior team members and collaborate with cross-functional departments to ensure data quality and process efficiency.
The role involves preparing programming scripts to generate NONMEM analysis datasets and managing e-submission packages for PK/PD modeling. You will also provide guidance to junior team members and collaborate with cross-functional departments to ensure data quality and process efficiency.
Lead statistical activities for clinical trials from protocol design to reporting while collaborating with cross-functional teams. Provide oversight for internal programming and CRO contributions while utilizing advanced statistical methods and machine learning to derive actionable insights.
You will provide statistical strategy and oversight for clinical trials, including the design of protocols, SAPs, and regulatory documentation. Additionally, you will manage external CRO activities and leverage advanced statistical methods and machine learning to drive actionable insights.
Lead statistical activities for assigned clinical trials from protocol design to reporting while representing the statistics function on cross-functional teams. Provide expert statistical support for clinical development plans and oversee internal programming activities or CRO contributions.
The Principal Statistical Programmer will independently manage clinical trial reporting activities, including the generation of SDTM and ADaM datasets and complex statistical outputs. They will also oversee CRO programming deliverables and ensure compliance with FDA regulations and clinical development standards.
Develop and validate SAS and/or R programs, specifications, datasets, tables, listings, graphs, and regulatory documentation for clinical trials. Oversee CRO programming deliverables, support regulatory submissions and study reports, and collaborate with internal and external teams to meet quality standards and timelines.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials while ensuring compliance with CDISC standards. They will also lead project tasks, generate submission documents, and collaborate with cross-functional teams to meet project deadlines.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials while generating and validating SDTM and ADaM datasets. They will also communicate with cross-functional teams and clients to manage project specifications and submission documentation.
The Principal Statistical Programmer provides technical and project management leadership for SAS programs and clinical trial data analysis. They ensure compliance with regulatory standards and oversee the production of SDTM and ADaM datasets for electronic submissions.
The Clinical Insights Analyst supports cross-functional teams in identifying and managing clinical trial risks through the implementation of Key Risk Indicators and Quality Tolerance Limits. They are responsible for maintaining the Risk-Based Quality Management system, analyzing data anomalies, and ensuring inspection readiness.
The Biostatistician will provide statistical support for clinical studies, including protocol development, sample size calculations, and the creation of statistical analysis plans. They will also perform exploratory analyses, interpret results, and prepare clinical study reports for regulatory submissions.
The Principal Biostatistician will lead Phase I-IV clinical studies, providing strategic statistical guidance and developing study protocols. They will also utilize advanced statistical methods, machine learning, and deep learning to analyze data and automate processes for clinical development.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials while generating and validating SDTM and ADaM datasets. They will also lead project tasks, communicate with cross-functional teams, and ensure high-quality submission deliverables.
The Senior Biostatistician will provide statistical support for clinical trials, including protocol development, sample size calculations, and the creation of statistical analysis plans. They will also perform statistical analyses, interpret results, and prepare clinical study reports for regulatory submissions.
Program, analyze, and report clinical trial safety and efficacy data using SAS, including generating and validating SDTM and ADaM datasets and tables, listings, and figures. Support or lead clinical studies, prepare submission documents, produce ad-hoc reports, and coordinate with client and cross-functional teams on specifications, status, and issues.
Lead or support clinical data management study activities, CRO oversight, and delivery timelines while coordinating with client stakeholders and cross-functional teams to ensure high-quality, timely data deliverables. Manage vendor budgets and risks, maintain operational processes and inspection-ready records, and contribute to regulatory readiness, governance, and continuous improvement.
Lead and mentor a team of health economists while serving as a technical and strategic lead on client projects involving economic modeling, data analysis, pricing, reimbursement, market access, and health technology assessment submissions. Oversee project quality and delivery, support staffing and operational planning, improve processes, and contribute to proposals, marketing, and conference activities.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials using SAS while ensuring compliance with CDISC standards. They will also generate and validate datasets, tables, listings, and figures, and support submission documentation for regulatory purposes.
The Associate Director will provide statistical leadership and support for clinical trials within a pharmaceutical client's global therapeutic group. Responsibilities include developing clinical trial protocols, overseeing vendor deliverables, and utilizing advanced statistical methods and machine learning to derive actionable insights.
The Director of Business Development is responsible for driving revenue growth and managing customer relationships within the DACH territory. They will act as a trusted advisor to clients, evangelizing the company's vision and implementing effective go-to-market strategies.
The role involves supporting the Epidemiology team by preparing Real World data and conducting statistical analysis to inform clinical development and safety documents. You will also partner with stakeholders to manage projects and provide technical expertise for observational studies.
The Associate Director provides senior technical leadership and functional guidance for epidemiological programming, ensuring high-quality, reproducible outputs for real-world evidence studies. They also manage programming strategies, mentor team members, and collaborate with cross-functional partners to support complex research objectives.
The role involves leveraging advanced SAS programming and CDISC standards to support or lead Phase I-IV clinical trials for a global pharmaceutical client. Responsibilities include data manipulation, analysis, and reporting within a globally dispersed team environment.
The Principal Statistical Programmer implements reporting and analysis activities for sponsor clinical trials while providing expert technical support to team members. They are also responsible for overseeing CRO programmers to ensure high-quality and consistent data summaries.
