Manager, Biostatistics - Hematology

Regeneron Pharmaceuticals; Tarrytown (GA); On-site; USD 129,000 - 210,000; Full time

Job summary

Regeneron Pharmaceuticals in the United States seeks a Manager in Biostatistics Hematology to support Clinical Biostatistics within Global Development. You will work with cross-functional teams to articulate questions, design studies, and frame statistical approaches, co‑author protocols and SAPs, and influence regulatory decisions.

You will develop training, advance infrastructure, and contribute to publications while collaborating with Medical Directors and Regulatory Affairs.

Qualifications

• PhD or MS in statistics/biostatistics with relevant industry experience.
• Experience in drug development and regulatory context.
• Proven leadership and cross-functional collaboration.
• Proficiency in R or SAS.

Responsibilities

• Collaborate with cross-functional teams to design and analyze clinical trials.
• Develop protocols and statistical analysis plans; specify methodologies.
• Co‑author SAS/R outputs, tables, figures for regulatory reporting.
• Provide training and contribute to infrastructure improvements.

Skills

Leadership

Cross-functional collaboration

Communication

Critical thinking

Education

PhD in statistics/biostatistics

MS in statistics/biostatistics

Tools

R

SAS

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 to join our Biostatistics Hematology team. This position is for a qualified Statistician/Biostatistician to support Clinical Biostatistics within Global Development.

The incumbent will work with cross-functional teams to articulate drug development questions, assess the feasibility of endpoints and frame statistical approaches to address those questions, design clinical experiments and interventional studies to generate and analyze the resulting data, and work with teams to appropriately interpret the results and make decisions. The incumbent will co-author clinical study protocols, statistical analysis plans, and perform statistical analyses for interim and final reports. The incumbent will also develop and deliver training to non-statistical colleagues, collaborate on development of new infrastructure and processes, and influence the external pharmaceutical industry and regulatory environment through participation in professional associations, conferences, and publications.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

• Work Location: Tarrytown, NY or Warren, NJ
• 4 days per week on site
• 25% Travel may be required

Discover your role:

• Interacting with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.
• Developing individual protocols and statistical analysis plans and determines appropriate statistical methodology for data analysis.
• Collaborating with Statistical Programming on the programming of tables, figures and listings to support decision making and for regulatory reporting.
• Evaluating appropriateness of available software for planned analyses and determines needs for use of novel statistical methodology or tools.
• Analyzing data and interprets results from clinical trials and of data from non-trial sources to facilitate program-level decision making.
• Preparing presentations and written reports to effectively communicate results to the project team, management, and regulatory agencies. Co-presents findings to management.
• Is involved in research activities for innovative statistical methods and applications in clinical trial development as well as providing training to non-statisticians.

This role requires:

• PhD or equivalent degree in statistics/biostatistics with >2 years’ experience in the pharmaceutical industry, or MS degree in statistics/biostatistics with >7 years’ experience.
• Knowledge of drug discovery and development and ability to integrate statistical concepts into drug discovery and development strategies.
• Excellent influence and leadership skills, and a demonstrated ability to collaborate in a cross-functional environment.
• Must be able to work productively in a fast-paced collaborative environment, with demonstrated critical thinking skills, time management skills, and effective communication skills.
• Solid knowledge of statistical analysis methodologies, experimental and clinical trial design
• Expertise in statistical software such as R or SAS is required

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.

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.

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)

$128,600.00 - $210,000.00