Implement the vision for data and analysis infrastructure platforms to support data flow from collection to submission. Coordinate the design and delivery of technical solutions to enable an open-source programming ecosystem.
Cytel
19 Remote Job Openings at Cytel
Lead Phase I-IV clinical studies by providing statistical expertise for protocols, clinical development plans, and concept sheets. Formulate integrated analytical approaches using statistical methods and machine learning to discover actionable insights and automate processes.
The analyst will work embedded within a pharmaceutical client to drive innovation in patient treatment. They will focus on applying data analytics and visualization to clinical trial data to support study design and risk management.
The Clinical Data Manager II provides comprehensive data management support for clinical studies. They are responsible for ongoing data review to ensure accuracy, completeness, and consistency according to study protocols.
Lead consulting engagements for pharmaceutical and biotechnology clients to define optimal regulatory and clinical pathways. Provide strategic guidance and thought leadership to accelerate patient access to health technologies.
Associate Counsel – Software Licensing & Commercial Contracts (preference Research Triangle Area)
Cytel
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Full Time
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12 days ago
Cytel
Provide legal guidance on software licensing, SaaS agreements, and commercial transactions to support business growth. Partner with sales, product, and executive teams to negotiate complex agreements and mitigate legal risks.
Principal Biostatistician - Chemistry, Manufacturing and Control -
Cytel
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Full Time
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13 days ago
Cytel
Support CMC projects across the drug development lifecycle by analyzing complex manufacturing data. Ensure product quality, consistency, and regulatory compliance for a global pharmaceutical client.
The role involves supporting vaccine projects across the drug development lifecycle by analyzing complex manufacturing data. The biostatistician will ensure product quality, consistency, and regulatory compliance while working embedded within a pharmaceutical client.
Define and execute a global IT strategy and roadmap to drive business performance and digital transformation. Oversee IT operations, infrastructure, cybersecurity, and enterprise applications while leading a high-performing global team.
The Project Finance Analyst serves as the finance lead for assigned studies to support project teams. They are responsible for aligning project financial activities with the broader financial goals of the organization.
Principal Biostatistician FSP - Late Phase Immunology and Neurology
Cytel
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Full Time
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20 days ago
Cytel
Lead Phase I-IV clinical studies and provide statistical expertise for clinical development plans, protocols, and concept sheets. Formulate integrated analytical approaches using statistical methods and machine learning to discover actionable insights and automate processes.
The role involves implementing reporting and analysis activities for sponsor clinical trials and overseeing CRO programmers to ensure high-quality data summaries. The individual will work independently to provide expert technical support and track progress within a pharmaceutical client 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.
The Principal Statistical Programmer will implement reporting and analysis activities for sponsor clinical trials while providing expert technical support to team members. They will also oversee CRO programmers to ensure high-quality and consistent delivery of data summaries.
The Senior Statistical Programmer will lead or support Phase I-IV clinical trials by leveraging advanced SAS programming and CDISC standards. They will be embedded within a pharmaceutical client to drive innovation in patient treatment through data analysis and reporting.
The Principal Statistical Programmer will implement reporting and analysis activities for sponsor clinical trials and provide expert technical support to team members. They will also oversee CRO programmers to ensure high-quality and consistent delivery of data summaries.
The Senior Statistical Programmer will lead or support Phase I-IV clinical trials by leveraging advanced SAS programming and CDISC standards. They will be embedded within a pharmaceutical client to drive innovation in patient treatment through data analysis and reporting.
The Principal Statistical Programmer implements reporting and analysis activities for sponsor clinical trials and provides expert technical support to team members. They are also responsible for overseeing CRO programmers to ensure high-quality and consistent data summaries.
The Senior Statistical Programmer will leverage advanced SAS programming and CDISC standards to support or lead Phase I-IV clinical trials. This role involves working fully embedded within a pharmaceutical client to drive innovation in patient treatment.
