Cytel

Statistical Programmer I FSP

Cytel  •  United States (Onsite)  •  3 hours ago
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Job Description

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 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:

We are looking for a Recent Graduate to perform and act as a Statistical Programmer, where you will leverage your education to develop and expand programming skills, supporting one or more Phase I-IV clinical trials. This is a great opportunity to start a career in Clinical Life Sciences, supported by Cytel and embedded in a trusted partner.

As a Statistical Programmer, your responsibilities will include:

  • Performing data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
  • Applying your SAS programming skills, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s)
  • Generating ad-hoc reports
  • Preparing and validating submission packages
  • Applying your understanding/experience with Efficacy analysis
  • Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
  • Being adaptable and flexible when priorities change

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

  • A minimum of 4 years of Undergraduate study and 2 additional years of Graduate-level education
  • Academic training in both of the following 2 categories (or closely related fields)
  • Statistics, Epidemiology, or Data Science
  • Computer Science, Mathematics, or Computational Science
  • Foundational data manipulation, analysis and reporting skills
  • Familiarity with drug development life cycle and a passion to learn and expand knowledge
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Excellent oral and written English communication skills
  • Ability to provide quality output and deliverables, in adherence with challenging timelines
  • Willingness and ability to learn and follow Company’s standard processes and procedures.
  • Ability to effectively learn and perform statistical programming and related tasks
Cytel

About Cytel

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.

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Cambridge, MA
Year Founded
1987
Website
cytel.com
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