Principal Statistical Programmer

Regeneron
Warren, NJ, United States
1 day ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Experienced
Experience required
3 years minimum
Compensation
$109,900.0 - $179,300.0
Working hours
Regular working hours

Tech stack

Computer Programming Coherent Remote File System (CRFS) Maintaining Code

Job description

  • 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

Requirements

  • 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

Benefits & conditions

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, and 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. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.

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

About the company

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, Regeneron is a leading biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases. Founded and led by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to numerous approved treatments and product candidates in development, most 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, neurological diseases, hematologic conditions, infectious diseases, and rare diseases.

Apply for this position

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Apply on www.biospace.com
Prepare application

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