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.
Cytel
25 Remote Job Openings at Cytel
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.
Lead strategic consulting engagements by providing quantitative guidance on clinical development plans and regulatory strategies. Drive thought leadership in model-informed drug development to help clients optimize regulatory and clinical pathways.
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 role involves leading or supporting Phase I-IV clinical trials by leveraging advanced SAS programming and CDISC standards. The programmer will be embedded within a pharmaceutical client to deliver high-quality data manipulation, analysis, and reporting.
Sr Proposal Operations Mgr (Remote - MUST have CRO contracting exp.)
Cytel
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Full Time
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15 days ago
Cytel
Provide technical support to the Proposals & Contracts group in preparing and managing deliverables. Partner with Subject Matter Experts to enhance and update tools for Finance and Project Management staff.
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 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. The role involves working embedded within a pharmaceutical client to drive innovation and patient treatment solutions.
The Senior Clinical Programmer will support the creation, validation, and execution of clinical study data. They will manage clinical data workflows and ensure data integration across various clinical trial systems.
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 embedded within a pharmaceutical client to drive innovation in patient treatment.
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 embedded within a global pharmaceutical client to drive innovation in patient treatment.
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.
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.
The Principal Statistical Programmer will work independently to implement reporting and analysis activities for sponsor clinical trials. They will also oversee CRO programmers to ensure high-quality data summaries are delivered consistently across various therapeutic areas.
The Principal Biostatistician will lead Phase I-IV clinical studies and provide statistical expertise for clinical development plans and protocols. They will also utilize advanced statistical methods, machine learning, and deep learning to discover actionable insights and automate processes.
The Principal Statistical Programmer will work independently to implement reporting and analysis activities for sponsor clinical trials. They will also provide expert technical support to team members and oversee CRO programmers to ensure high-quality data summaries.
Manage the end-to-end sales cycle from lead generation to deal closure while collaborating with stakeholders at all levels. Drive pipeline development by leveraging an established network and working cross-functionally with internal commercial and operational teams.
The Senior Statistical Programmer will leverage advanced SAS programming and CDISC standards to support or lead Phase I-IV clinical trials. The role involves working fully embedded within a pharmaceutical client to drive innovation in patient treatment.
The candidate will manage clinical data programming, focusing on data integration and the execution of clinical study data. They will also be responsible for validating clinical trial systems and ensuring data integrity in a fast-paced environment.
You will support the epidemiology team by preparing real-world data, conducting statistical analysis, and creating algorithms for observational studies. Additionally, you will collaborate with internal and external stakeholders to manage projects and ensure timely delivery of high-quality analytical insights.
The Senior Statistical Programmer will leverage advanced SAS programming and CDISC standards to support or lead Phase I-IV clinical trials. The role involves working fully embedded within a pharmaceutical client to drive innovation in patient treatment.
Executive Consultant – Vice President, Quantitative Clinical Pharmacology
Cytel
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Full Time
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2 months ago
Cytel
This role involves blending scientific leadership, strategic advisory, and technical excellence in quantitative clinical pharmacology to guide clients in shaping optimal regulatory and clinical development pathways. The consultant will leverage deep quantitative expertise and business acumen to expand thought leadership and drive complex consulting engagements.
The Principal Statistical Programmer will implement all reporting and analysis activities for Sponsor clinical trials, working independently with minimal supervision. This role involves tracking progress and providing expert technical support while overseeing CRO programmers to ensure high-quality data summaries.
The Principal Biostatistician will provide statistical and development support for client trials, influencing processes, clinical development plans, and protocols, potentially overseeing work from other vendors. They will formulate integrated analytical approaches using advanced methods like machine learning and deep learning to extract insights and automate repetitive processes.