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Cytel

Associate Director, Epidemiological Statistical Programming FSP

Jefferson City, MO, United States

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Job details

Posting language: English

Original job description

Summary

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.

As an Associate Director, Epidemiological Statistical Programming, your responsibilities will include:

+ Provide technical and functional leadership to statistical programmers supporting epidemiological and real-world evidence (RWE) studies, including mentoring team members, providing technical guidance, and promoting consistent, high-quality programming practices.

+ Lead and contribute hands-on to statistical programming activities for epidemiological studies across multiple therapeutic areas, translating study objectives, protocols, and statistical analysis plans into robust and reproducible analytical solutions.

+ Develop, validate, and maintain high-quality SAS and/or R programs to support the creation of analysis datasets, statistical outputs, tables, figures, and other data products required for epidemiological research and evidence generation.

+ Partner closely with epidemiologists, statisticians, data scientists, and other cross-functional stakeholders to determine appropriate programming approaches and ensure analyses are implemented accurately and efficiently.

+ Provide expert technical consultation on complex programming, data, and analytical challenges, identifying appropriate solutions and advising team members and project stakeholders on best practices.

+ Oversee and review programming deliverables to ensure accuracy, reproducibility, consistency, quality, and adherence to agreed timelines and standards.

+ Support programming activities using a variety of real-world and observational data sources, which may include administrative claims, electronic health records, registries, and other healthcare databases.

+ Lead or contribute to the development of analysis-ready datasets and programming specifications, including data transformations, derivation logic, quality-control procedures, and documentation necessary to ensure transparent and reproducible analyses.

+ Establish, enhance, and promote programming standards, reusable tools, macros, code libraries, documentation, and quality-control processes that improve efficiency and consistency across epidemiological projects.

+ Drive continuous improvement and identify opportunities for automation, standardization, and innovative programming approaches that enhance the scalability and quality of epidemiological programming activities.

+ Contribute to the planning and prioritization of programming activities across projects, proactively identifying resource needs, technical risks, dependencies, and potential challenges to successful delivery.

+ Support scientific deliverables including regulatory and health authority requests, publications, abstracts, presentations, evidence-generation activities, and other analyses supporting clinical development, medical affairs, and/or value and access objectives.

+ Ensure programming activities are conducted in accordance with applicable regulatory requirements, company policies, SOPs, data privacy requirements, and industry best practices.

+ Lead or contribute to the development and maintenance of SOPs, work instructions, programming conventions, and other documentation governing epidemiological statistical programming activities.

+ Foster strong collaboration across internal and external teams and contribute to the development of programming talent through coaching, knowledge sharing, technical review, and mentorship.

Here at Cytel, we want our employees to succeed, and we enable that success through consistent training, development, and support. To be successful in this position, you will have:

+ Bachelor's degree or higher in Statistics, Biostatistics, Epidemiology, Computer Science, Data Science, Mathematics, or a related quantitative discipline; advanced degree is a plus.

+ 8+ years of relevant statistical programming experience within the pharmaceutical, biotechnology, CRO, healthcare, or life sciences industry, with demonstrated experience supporting epidemiological, observational, real-world evidence (RWE), HEOR, and/or related research.

+ Experience with Optum and Truveta.

+ Advanced programming expertise in SAS and/or R, with demonstrated ability to develop, validate, and maintain complex analytical programs and reproducible programming workflows.

+ Strong experience working with large and complex healthcare data sources, such as administrative claims, electronic health records (EHR), patient registries, or other real-world data sources.

+ Demonstrated understanding of epidemiological study designs, statistical analysis methods, and the application of programming techniques to observational and real-world research.

+ Proven ability to provide technical leadership and guidance to statistical programmers, including mentoring colleagues, reviewing programming approaches and deliverables, and resolving complex technical challenges.

+ Experience leading or coordinating programming activities across multiple projects, including prioritizing deliverables, identifying risks and...

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