Associate Director, Epidemiological Statistical Programming FSP

United States · Remote ok

About this role

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 Associate Director, Epidemiological Statistical Programming serves as a senior technical leader within the Epidemiology programming function, providing functional guidance, technical expertise, and mentorship to statistical programmers while also contributing directly to complex epidemiological projects. Working with a high degree of independence, this individual translates project and scientific objectives into effective programming strategies, proactively manages priorities and deliverables, and provides expert technical consultation to team members and cross-functional partners.
 

The Associate Director is responsible for leading and supporting the implementation of statistical programming activities across epidemiological and real-world evidence studies, ensuring that analyses and data outputs are accurate, reproducible, consistent, and delivered to a high standard of quality. This role may provide technical oversight of internal and external programming resources, including CRO partners, and will establish and promote programming standards, efficient processes, and best practices across projects.

In addition to hands-on project responsibilities, the Associate Director will play an important role in developing programming capabilities within the team by mentoring colleagues, reviewing and advising on technical approaches, identifying opportunities for process improvement and automation, and helping ensure appropriate allocation and execution of programming work. The individual will collaborate closely with epidemiologists, statisticians, data scientists, and other cross-functional partners to support the generation of high-quality evidence across multiple therapeutic areas.


 

Company at a glance

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.

Founded1987
Team Size1,001-5,000 employees
WorkspaceRemote ok
IndustryPharmaceutical Manufacturing
Location
United States
Websitecytel.com
LinkedInLinkedIn

Top Benefits

  • Professional growth
  • Training and development

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