Cytel is a leading data-science CRO that enhances drug development and patient outcomes through innovative analytics, adaptive trial design, and comprehensive clinical trial services.
Cambridge, MA
Cytel is the world’s leading data-science CRO, driving advancements in human health through robust analytics and innovative clinical trial software. For nearly four decades, we have set the standard in adaptive trial design, leveraging extensive data insights to inform strategy throughout every phase of drug development and commercialization. Our mission is clear: accelerate drug development, enhance success rates, and deliver better patient outcomes. With a comprehensive suite of services from innovative trial design to end-to-end biometrics and real-world evidence, our specialized, multidisciplinary team ensures optimal strategies for preclinical research, trial execution, market access, and reimbursement. Headquartered in Cambridge, Massachusetts, Cytel has a global presence with over 2,000 employees across North America, Europe, and Asia. Learn more about how Cytel is harnessing the power of data to advance human health at www.cytel.com.
Remote · Canada
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.
Remote
Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview: This position reports to the Director, Biostatistics and Programming in the FSP Services busine…
Remote · Canada, United States
Lead and mentor a team of health economists while serving as a technical and strategic expert on health economics projects, including economic modeling, data analysis, and local HTA submissions. Oversee project delivery and client deliverables, support departmental operations and process improvement, and contribute to business development through proposals, marketing, and conference activities.
On-site
Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview: The Principal Statistical Programmer works independently with only concept level instruction an…
On-site
Who Are You? A Project Manager with experience working in pharmaceutical and clinical development environment. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. You never settle for what is, but always push clinical development forward to what it could be. You motivate others to do the same. Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Project Manager you will be dedicated to one of our…
On-site
The role involves providing statistical programming and data analytic support to the Epidemiology team using Real World Data. Key duties include creating analytical databases, conducting statistical analyses, and producing reports for regulatory and safety documents.
On-site
The Associate Director provides technical leadership and mentorship to statistical programmers while executing complex epidemiological and real-world evidence studies. They are responsible for developing reproducible analytical solutions and ensuring the quality and accuracy of data outputs across multiple therapeutic areas.
On-site
The Principal Statistical Programmer will provide technical expertise for statistical programming across clinical trials and support the development of statistical analysis and reporting deliverables. They will collaborate with various stakeholders to ensure project plans are executed efficiently and deliver high-quality outputs.
