Lead Phase I-IV clinical studies by providing statistical expertise for clinical development plans, protocols, and concept sheets. Formulate integrated analytical approaches using machine learning and deep learning to discover actionable insights and automate processes.
Cytel
29 Remote Job Openings at Cytel
Lead or support Phase I-III clinical studies with a specific focus on Alzheimer's and Type 2 Diabetes. Work within the FSP department to provide biostatistics services for various clients.
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.
Lead statistician responsible for the design, analysis, and reporting of Phase I to IV clinical studies and regulatory filings. Collaborates across multiple clinical development functions to execute statistical strategies and ensure scientifically sound study documentation.
Lead consulting engagements for pharmaceutical and biotechnology clients to define optimal regulatory and clinical pathways. Strengthen the company's reputation for innovation and thought leadership in biostatistics while managing long-term client relationships.
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.
Lead key accounting areas including revenue recognition and strategic initiatives while enhancing internal controls following an ERP implementation. The role involves auditing project set-ups, reviewing customer contracts, and collaborating with senior leadership.
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 role involves working as a dedicated Senior Clinical Data Manager embedded within a pharmaceutical client to drive innovation in patient treatment. Responsibilities include managing clinical trial data and collaborating across functional interfaces within the drug development process.
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 manipulation 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 Medical Coder ensures accurate and consistent coding of medical terms using standardized dictionaries to support clinical trials. They collaborate with cross-functional teams to maintain high-quality data that meets global regulatory standards.
The Project Finance Analyst serves as the finance lead for assigned studies to support project teams financially. They are responsible for aligning project financial activities with the broader financial goals of the organization.
Design, develop, and maintain clinical databases using Medidata Rave to translate protocol requirements into high-quality EDC solutions. Collaborate with data management and biostatistics teams to deliver scalable database builds for clinical trials.
Perform statistical analyses to support clinical trial and marketed product submissions to regulatory agencies. Lead or support Phase I-IV clinical studies while collaborating closely with pharmaceutical clients.
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 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.
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 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 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.
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.
Executive Consultant – Vice President, Quantitative Clinical Pharmacology
Cytel
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Full Time
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3 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 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.