Mgr Biostatistics-, Genetics Medicine and Rare Disease

Regeneron Pharmaceuticals
Location
TARRYTOWN
Job Type
Full-time
Posted
November 13, 2026
Salary Range
$131k - $214k USD

Job Description

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 Manager Biostatistics Genetics Medicine & Rare Disease to join our Biostatistics Genetics Medicine and Rare Disease team, supporting Global Development in a hybrid work model. In this role, you will provide statistical leadership for clinical development programs while collaborating with Medical Directors, Clinical Scientists, Regulatory Affairs, Statistical Programming, Data Management, and Medical Writing. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where

Tarrytown, NY; Uxbridge, UK; or Cambridge, US

Work model: Hybrid

Discover your role

  • Partner with cross-functional teams to design and analyze clinical trials.
  • Develop clinical study protocols, statistical analysis plans, and statistical methodologies.
  • Collaborate with Statistical Programming on tables, figures, and listings for reporting.
  • Analyze clinical and non-trial data to support program-level decisions.
  • Interpret results and communicate findings through reports, presentations, and regulatory materials.
  • Evaluate software and recommend novel statistical methods or analytical tools.
  • Contribute to statistical innovation, infrastructure, process development, and training activities.
  • You thrive in a collaborative environment and influence decisions through scientific insight.

This role requires

  • PhD in Statistics/Biostatistics with 2+ years of pharmaceutical industry experience; or MS with 7+ years.
  • Knowledge of drug discovery and development and application of statistical strategies.
  • Solid expertise in statistical analysis methodology, experimental design, and clinical trial design.
  • Proficiency with statistical software such as R or SAS.
  • Experience developing protocols, statistical analysis plans, and clinical study analyses.
  • Ability to interpret data and support regulatory reporting and decision-making.
  • Strong leadership, influence, collaboration, communication, critical thinking, and time management skills.
  • Ability to work effectively in a fast-paced cross-functional environment.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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, 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.

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 Manager Biostatistics Genetics Medicine & Rare Disease to join our Biostatistics Genetics Medicine and Rare Disease team, supporting Global Development in a hybrid work model. In this role, you will provide statistical leadership for clinical development programs while collaborating with Medical Directors, Clinical Scientists, Regulatory Affairs, Statistical Programming, Data Management, and Medical Writing. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where

Tarrytown, NY; Uxbridge, UK; or Cambridge, US

Work model: Hybrid

Discover your role

  • Partner with cross-functional teams to design and analyze clinical trials.
  • Develop clinical study protocols, statistical analysis plans, and statistical methodologies.
  • Collaborate with Statistical Programming on tables, figures, and listings for reporting.
  • Analyze clinical and non-trial data to support program-level decisions.
  • Interpret results and communicate findings through reports, presentations, and regulatory materials.
  • Evaluate software and recommend novel statistical methods or analytical tools.
  • Contribute to statistical innovation, infrastructure, process development, and training activities.
  • You thrive in a collaborative environment and influence decisions through scientific insight.

This role requires

  • PhD in Statistics/Biostatistics with 2+ years of pharmaceutical industry experience; or MS with 7+ years.
  • Knowledge of drug discovery and development and application of statistical strategies.
  • Solid expertise in statistical analysis methodology, experimental design, and clinical trial design.
  • Proficiency with statistical software such as R or SAS.
  • Experience developing protocols, statistical analysis plans, and clinical study analyses.
  • Ability to interpret data and support regulatory reporting and decision-making.
  • Strong leadership, influence, collaboration, communication, critical thinking, and time management skills.
  • Ability to work effectively in a fast-paced cross-functional environment.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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, 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 on‑site. Please speak with your recruiter and hiring manager for more information about on‑site 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)

$131,200.00 - $214,200.00

Researching Regeneron before you apply?

See 25 open roles · Verified H-1B salary data · Clinical-trial hiring momentum · Culture, benefits & locations.

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Frequently Asked Questions

Where is this job located, and is it remote, hybrid, or on-site?
The role is listed in Tarrytown, NY, and can also be based in Uxbridge, UK, or Cambridge, US. It follows a hybrid work model. Regeneron says on-site expectations vary by role and location, so check with your recruiter and hiring manager.
What qualifications and experience do I need?
You need either a PhD in Statistics/Biostatistics with 2+ years of pharmaceutical industry experience or an MS with 7+ years. You also need expertise in statistical methodology, experimental design, and clinical trial design, proficiency in R or SAS, and experience developing protocols, statistical analysis plans, and clinical study analyses.
What will I be doing day to day?
You will design and analyze clinical trials with cross-functional teams and develop protocols, statistical analysis plans, and methodologies. You will work with Statistical Programming on tables, figures, and listings. You will analyze clinical and non-trial data, communicate findings in reports and regulatory materials, and recommend novel statistical methods or tools.
What is the salary range?
The posted range is $131,200 to $214,200 per year. The final offer depends on the country of employment, the specific role level, and your skills and experience.
What benefits are offered?
Depending on country and role, benefits may include annual bonuses or incentive plans, equity awards, and pension or retirement benefits. They may also include a 401(k) match, health and wellness programs, fitness centers, medical, dental, vision, life, and disability insurance, paid time off, and family support benefits.
Which team will I be part of and who will I work with?
You will join the Biostatistics Genetics Medicine and Rare Disease team, which supports Global Development. You will collaborate with Medical Directors, Clinical Scientists, Regulatory Affairs, Statistical Programming, Data Management, and Medical Writing.
Are there background checks as part of hiring?
Yes. Background checks may be conducted in line with the laws of the country where the position is based. They verify information such as identity, right to work, and educational qualifications before employment starts.

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  • 25 open roles
  • Verified H-1B salary data
  • Clinical-trial hiring momentum
  • Culture, benefits & locations
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Job Information

Source: manual
AI Relevance: 93/100 (Highly relevant)
Remote Type: onsite
Skills & Tags:
regeneron pharmaceuticals drug discovery biostatistics clinical

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