Principal Statistical Programmer in Cambridge

Principal Statistical Programmer in Cambridge

Cambridge Full-Time 54000 - 66000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Lead programming for clinical trial data and collaborate with a multidisciplinary study team.
  • Company: Join Regeneron, a science-driven company making life-changing medicines.
  • Benefits: Competitive salary, bonuses, health benefits, and wellness programs.
  • Other info: Inclusive culture with opportunities for professional growth and development.
  • Why this job: Make a meaningful impact on patients while advancing your career in a dynamic environment.
  • Qualifications: Master’s degree and 3+ years of programming experience in clinical studies.

The predicted salary is between 54000 - 66000 £ per year.

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.

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

This role might be for you if you:

  • 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, colour, 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.

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, health and wellness programs, fitness centres, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits.

Principal Statistical Programmer in Cambridge employer: Regeneron Pharmaceuticals

Regeneron is an exceptional employer, offering a dynamic work environment where innovation and collaboration thrive. As a Sales Specialist in Oncology, you will have the opportunity to engage with healthcare professionals and contribute to a growing oncology portfolio while benefiting from a comprehensive rewards package, including competitive bonuses and health programs. With a strong commitment to inclusivity and employee development, Regeneron fosters a culture that empowers you to excel in your career while making a meaningful impact in the healthcare sector.

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Contact Details:

Regeneron Pharmaceuticals Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Principal Statistical Programmer in Cambridge

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We think you need these skills to ace Principal Statistical Programmer in Cambridge

Statistical Programming
Clinical Trial Data Processing
Programming Logic Design and Testing
Documentation Skills
Quality Control
Collaboration within Multidisciplinary Teams
Creation of Programming Specifications

Some tips for your application 🫡

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How to prepare for a job interview at Regeneron Pharmaceuticals

Brush Up on Lab Techniques

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