261 Sas jobs available for remote work from home. Apply for positions such as Principal Statistical Programmer, Statistical Programmer II, Senior Statistical Programmer, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Principal Statistical Programmer will lead statistical programming teams to deliver clinical trial projects within budget and timelines while ensuring high-quality technical output. They will also provide mentorship, manage stakeholder relationships, and ensure compliance with regulatory standards and internal SOPs.
The Statistical Programmer II is responsible for creating derived datasets, tables, figures, and listings while ensuring high-quality service and regulatory compliance. They also assist in project start-up activities and provide mentorship to staff and project teams.
The Senior Statistical Programmer will lead statistical programming teams to deliver high-quality clinical study outputs within established timelines and budgets. They are responsible for overseeing project resourcing, ensuring regulatory compliance, and providing technical mentorship to staff.
The Associate, Model Development supervises the creation and maintenance of sophisticated empirical credit scoring models to support business decision-making. They also analyze trends, manage large datasets, and provide executive-level summaries to senior management.
The Senior Statistical Programmer Consultant develops, validates, and maintains SAS programs for clinical study data analysis and reporting. They collaborate with cross-functional teams to ensure programming deliverables meet quality standards and project timelines.
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The Supervisor oversees a team of analysts to provide financial data, reporting, and actionable insights to the Healthcare Finance management team. They are responsible for managing recurring financial reports, reconciliations, and coordinating analytical support across various internal departments.
The Senior SAS Developer will design, develop, and maintain SAS solutions to facilitate secure data exchange between internal systems and external trading partners. They will also manage compliance and regulatory reporting while ensuring all processes adhere to HIPAA and data privacy standards.
The Clinical Data Manager leads and manages clinical studies to ensure data is collected, reported, and maintained accurately and securely. They act as the primary liaison for project teams and vendors while overseeing database development, validation, and ongoing data cleaning.
The Senior Clinical Data Manager leads end-to-end data management activities for clinical studies, ensuring quality, timelines, and budget adherence. They provide mentorship to junior staff, manage sponsor relationships, and oversee the implementation of study-specific data processes.
The role involves providing scientific leadership and statistical programming expertise to support cross-functional teams in clinical trials. Responsibilities include developing PopPK/PD datasets, ensuring compliance and quality, and contributing to e-submission packages.
The Senior Data Anonymization Programmer will provide expert programming for clinical data anonymization and regulatory disclosure activities. Responsibilities include developing complex macros, performing quality control on outputs, and ensuring compliance with SDTM and ADaM standards.
The Principal Programmer will lead clinical and non-clinical study programming activities, ensuring high-quality dataset production and regulatory compliance. They will provide scientific leadership, manage complex macros, and oversee the development of statistical analysis plans and regulatory documentation.
The Principal Programmer will lead clinical and non-clinical study programming, ensuring high-quality dataset production and regulatory submission compliance. They will provide scientific leadership, mentor team members, and manage complex programming tasks while adhering to project timelines.
The role involves providing scientific leadership and statistical expertise to support global pharmaceutical clients. Responsibilities include leading independent analyses, ensuring compliance with regulatory standards, and fostering team development.
The Senior Statistician will provide scientific leadership and statistical expertise for vaccine and MPD studies. They are responsible for ensuring compliance, quality, and governance while mentoring team members.
The principal programmer will lead programming activities across clinical and non-clinical studies, ensuring high-quality dataset production and regulatory submission support. Responsibilities include providing scientific leadership, managing QC strategies, and overseeing CRO deliverables.
The Principal Statistician will provide scientific leadership and statistical expertise for GI studies while supporting a global pharmaceutical client. Responsibilities include developing post-hoc analysis plans, ensuring compliance and quality, and mentoring team members.
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The Senior Statistician will lead statistical aspects of clinical trials, including the development of Statistical Analysis Plans and study documentation. They will oversee reporting teams, provide scientific leadership, and act as a consultant for pharmaceutical and biotech clients.
Develop and maintain trial-specific databases, including eCRFs and edit checks, while adhering to project timelines. Support the programming of reports and listings to ensure standardization for data review and analysis.
The role involves providing statistical expertise and scientific leadership while overseeing people development and governance. You will support complex oncology clinical trials by ensuring compliance and high-quality programming standards.
The role involves managing clinical and non-clinical trial data, including eCRF programming, clinical coding, and third-party data management. The coordinator will ensure database cleanliness and may act as a Lead Data Manager for non-complex studies.
The Principal Statistical Programmer provides lead programming support for complex clinical research projects and offers expert consultation on methodologies. They are responsible for delivering regulatory-compliant outputs, developing documentation, and mentoring junior staff.
You will act as a founding Solutions Architect in the Nordics, partnering with account executives to demonstrate the value of Cohere's AI technology to enterprise and government customers. This involves leading technical pilots, designing enterprise architectures, and serving as the primary technical liaison between customers and the product team.
The Statistical Scientist will contribute to study design, statistical analysis, and programming for Real World Evidence projects. They will also support scientific communication activities, including publications and conference presentations, while collaborating with cross-functional teams.
The Senior Statistical Programmer creates SAS programs to generate analysis datasets and tables, listings, and figures for clinical trials. They also provide technical expertise, ensure quality of deliverables, and support electronic submission preparation.
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The intern will conduct retrospective and prospective real-world evidence research projects across various disease areas. They will also assist in developing research proposals, managing large databases, and preparing study reports or conference submissions.
The Director will lead and advance statistical and data management programming activities for biosimilar studies while ensuring high-quality, compliant deliverables. They are responsible for establishing robust programming standards, mentoring staff, and driving efficiency through automation and process optimization.
Perform clinical data management activities including data review, query generation, and reconciliation to support project timelines. Collaborate with project teams to maintain data management documentation and ensure quality standards are met throughout the clinical trial process.
The biostatistician will collaborate with clinical investigators to design studies, develop protocols, and write statistical analysis plans. They are also responsible for performing statistical analyses, ensuring data safety, and reporting findings for regulatory bodies and peer-reviewed publications.
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