Principal Statistical Programmer - Genetic Medicines

Regeneron Pharmaceuticals, Inc (USA)

Kentucky

Presencial

USD 110 000 - 179 000

Tempo integral

Há 4 dias
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Resumo da oferta

Regeneron Pharmaceuticals, Inc. seeks a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio onsite in Warren, NJ or Cambridge, MA.

You will provide programming leadership and support for processing clinical trial data, designing and testing program logic while ensuring consistent, high-quality documentation, all while collaborating with a multidisciplinary study team to support analysis and reporting through regulatory

Qualificações

  • Master's degree with 3+ years of relevant experience.
  • Proven programming experience supporting clinical study data and analysis deliverables.
  • Strong documentation and quality control skills within a regulated environment.
  • Experience collaborating within a multidisciplinary study team.

Responsabilidades

  • Support or lead programming and quality control of analysis datasets, tables, listings, and graphs.
  • Coordinate activities and communicate shifting timelines and milestones to the study team.
  • Create and maintain programming specifications for analysis datasets across studies.
  • Support creation and validation of submission requirements, including annotated CRFs and define documents.
  • Work within a multidisciplinary study team to provide timely, quality support through regulatory approval and launch.
  • Provide programming support for presentations and statistical ad hoc requests, assisting with more complex data as needed.
  • Participate in department working groups, contributing to tool development and process improvement.
  • Design and test program logic independently, maintaining documentation in a regulated environment.
  • Enjoy working independently while staying closely connected to a broader study team.
  • Communicate clearly and proactively, especially around shifting timelines.
  • Take pride in accuracy and consistency when documenting and maintaining code.
  • Think analytically and enjoy solving programming and data challenges.
  • Stay curious about process improvement and enjoy contributing ideas to working groups.
  • Adapt comfortably to ad hoc requests and evolving priorities from senior leadership.
  • Bring attention to detail and a quality mindset to regulated work.

Conhecimentos

Programming experience
Analytical thinking
Documentation
Team collaboration

Formação académica

Master's degree

Ferramentas

SAS

Descrição da oferta de emprego

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will provide programming leadership and support for processing clinical trial data, designing and testing program logic while ensuring consistent, high-quality documentation, all while collaborating with a multidisciplinary study team to support analysis and reporting through regulatory approval and beyond. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

Location: Warren, NJ or Cambridge, MA

Work model/flexibility: onsite

Discover your role:
  • Support or lead programming and quality control of analysis datasets, tables, listings, and graphs
  • Coordinate activities and communicate shifting timelines and milestones to the study team
  • Create and maintain programming specifications for analysis datasets across studies
  • Support creation and validation of submission requirements, including annotated CRFs and define documents
  • Work within a multidisciplinary study team to provide timely, quality support through regulatory approval and launch
  • Provide programming support for presentations and statistical ad hoc requests, assisting with more complex data as needed
  • Participate in department working groups, contributing to tool development and process improvement
  • Design and test program logic independently, maintaining documentation in a regulated environment
  • Enjoy working independently while staying closely connected to a broader study team
  • Communicate clearly and proactively, especially around shifting timelines
  • Take pride in accuracy and consistency when documenting and maintaining code
  • Think analytically and enjoy solving programming and data challenges
  • Stay curious about process improvement and enjoy contributing ideas to working groups
  • Adapt comfortably to ad hoc requests and evolving priorities from senior leadership
  • Bring attention to detail and a quality mindset to regulated work
This role requires:
  • Master's degree with 3+ years of relevant experience
  • Proven programming experience supporting clinical study data and analysis deliverables
  • Strong documentation and quality control skills within a regulated environment
  • Experience collaborating within a multidisciplinary study team

We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship. Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role:

  • annual bonuses or other incentive plans
  • equity awards
  • pension or retirement benefits
  • 401(k) company match
  • health and wellness programs
  • fitness centers
  • insurance benefits (e.g. medical, dental, vision, life and disability)
  • paid time off
  • family support benefits

For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually) $109,900.00 - $179,300.00

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA-approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases. Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.

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