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Cytel

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We help life science leaders unlock the power of data, solve their toughest problems, and make evidence-driven decisions

Cambridge, MA

Pharmaceutical Manufacturing
1,001–5,000 people

About

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.

Open positions

Research Principal, Real World Evidence

On-site · Canada

Lead the generation of impactful real-world evidence focusing on comparative effectiveness research and external control arms. Manage client portfolios, oversee project execution, and mentor junior staff while contributing to research innovation strategy.

Market & Business Development Associate

On-site · Canada

The role focuses on generating new business opportunities through prospecting and lead generation for clinical trial biometric consulting and CRO services. It also involves managing end-to-end sales for software solutions and supporting business development directors with administrative tasks.

Associate Director, Real World Evidence

On-site · Canada

Responsible for initiating business opportunities and overseeing the drafting of proposals in collaboration with business development partners. Manages the delivery team to ensure high levels of client satisfaction within the RWE department.

Senior Biostatistician FSP (HTA, German-speaking)

On-site

Job Description Who Are You? An experienced German-speaking Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will support our customer's Health Technology Assessment (HTA) dossiers in Germany. You are motivated 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 behi…

Principal Biostatistician FSP - RWE - Remote

Remote · ["Canada"]

Job Description Cytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services. At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of drug development. In this role you will join our FSP department and will for our client, one of the top pharmaceutical companies. We are seeking a Senio…

Principal Biostatistician FSP

On-site · Canada

As a Principal Biostatistician, you will lead statistical activities for assigned clinical trials from protocol design to reporting of results. You will also represent the Statistics function on cross-functional teams and oversee programming activities.

Senior Director, Innovative Statistics

On-site · Canada

Provide strategic advice on client projects and develop innovative solutions by combining established methodologies with novel statistical approaches. Lead consulting accounts, build partnerships with clients, and contribute to thought leadership in statistical methodology.

Principal Statistical Programmer - SDTM team

On-site · Canada

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.