Director, Statistical Methodology

1 month ago


Princeton, New Jersey, United States Bristol Myers Squibb Full time
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: .

The Director of Statistical Methodology works closely with Head of Statistical methodology to implement vision and strategy of Statistical Methodology function within Global Biostatistics and Data Science organization. They will engage with Biostatisticians and other cross functional team members to drive development of statistical methods for emerging trial design and analysis problems. This individual will also mentor junior stats methodologists to help them grow their technical and soft skills.

While this position is primarily focused on statistical methods research and development, it also involves close collaboration with StuDIO ( S tudy D esign Innovation and Optimization) function within Global Biometrics and Data Sciences of BMS. StuDIO's mission is to support and enable development teams to pursue optimal design/development options with sharpened focus on scientific rigor and innovation, operational feasibility, and resource efficiency across the BMS portfolio. The accountability of the Director of Stat Methdology role would include (but not limited to) developing methodological solutions to problems identified via StuDIO in close collaboration with study teams.

Key Responsibilities Formulates, develops, implements innovative novel statistical analysis methods and innovative study designs across therapeutic areas. Translates scientific questions into statistical terms and statistical concepts into layman terms. Communicates findings of their project-driven research to cross-functional teams, provides interpretation of their scientific results in a manner accessible to non-statisticians. Functions as statistical lead on statistical topics influencing and advising senior leadership on issues that have business impact. Continually develops technical knowledge of statistical methodology and build BMS external scientific reputation via publications and presentations. Qualifications & Experience Ph.D. in Statistics/Biostatistics with 9+ years of experience Deep expertise in one of the following scientific topics (with proven publication records) and working knowledge of the others: Adaptive Design, Multiplicity, Bayesian Methods, including Dynamic Borrowing, Master Protocols, Non-Proportional Hazards, RWE/RWD, Advanced Predictive Modelling Working knowledge of scientific computing/programming (SAS, R or C++ and Bayesian packages) and implementation of advanced statistical analysis, data manipulation, graphing & simulation. Ability to summarize technically/analytically complex information for a non-technical audience Demonstrated ability to work in a team environment with good interpersonal, communication, writing and organizational skills. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients' lives through scienceTM , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit eeo -accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

  • Princeton, New Jersey, United States Bristol Myers Squibb Company Full time

    Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...


  • Princeton, New Jersey, United States Bristol Myers Squibb Full time

    Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...


  • Princeton, New Jersey, United States Bristol Myers Squibb Company Full time

    At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to...

  • Director Biostatistics

    3 months ago


    Princeton, New Jersey, United States Bristol Myers Squibb Full time

    Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...


  • Princeton, New Jersey, United States PMV Pharmaceuticals, Inc. Full time

    Director, Biostatistics & Data AnalyticsPMV Pharmaceuticals, Inc. is at the forefront of developing innovative p53 reactivators aimed at treating cancer. Our team comprises experts in the field, leveraging over thirty years of p53 biological research to merge scientific insights with a strong focus on pharmaceutical development.We are seeking a qualified...


  • Princeton, New Jersey, United States PMV Pharmaceuticals, Inc. Full time

    Director of Biostatistics & Data AnalyticsPMV Pharmaceuticals is at the forefront of developing innovative p53 reactivators aimed at combating cancer. By leveraging over thirty years of expertise in p53 biology, PMV Pharmaceuticals merges deep biological insights with a strong focus on pharmaceutical development.The organization is seeking a qualified...

  • Associate Director

    2 weeks ago


    Princeton, New Jersey, United States Novo Nordisk Full time

    About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product...


  • Princeton, New Jersey, United States Novo Nordisk Full time

    About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new...


  • Princeton, New Jersey, United States Cogentrix Full time

    Director- Risk ManagementJob Summary:Cogentrix is seeking a highly skilled Director of Risk Management and Compliance to lead the risk management function, including analysis, measurement, monitoring, and reporting of energy and commodity portfolio risks.Key Responsibilities:Design and Implement Risk Reporting: Develop and implement effective risk reporting...

  • Medical Director

    3 weeks ago


    Princeton, New Jersey, United States Novo Nordisk Full time

    About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product...


  • Princeton, New Jersey, United States System One Holdings, LLC Full time

    Title: Clinical Safety Analytics Associate Company: System One Holdings, LLC Location: Hybrid Type: Contract Overview System One Holdings, LLC is seeking a Clinical Safety Analytics Associate to join our team. This role is pivotal within the Pharmacovigilance Center of Excellence (PV CoE). The successful candidate will focus on analyzing clinical and safety...


  • Princeton, New Jersey, United States Life Science People Full time

    The Director of Process Development will spearhead the advancement, refinement, and scaling of viral vector production within the organization. This pivotal role encompasses overseeing a team of scientists and engineers dedicated to process development, ensuring the establishment of robust and scalable production methodologies, and collaborating with various...


  • Princeton, New Jersey, United States Life Science People Full time

    The Director of Process Development will spearhead the advancement, refinement, and scaling of viral vector production within the organization. This pivotal role encompasses overseeing a team of process development scientists and engineers, ensuring the establishment of robust and scalable production methodologies, and collaborating closely with various...


  • Princeton, New Jersey, United States Life Science People Full time

    The Director of Process Development will spearhead the advancement, refinement, and scaling of viral vector production within the organization. This pivotal role encompasses overseeing a team of process development specialists and engineers, ensuring the establishment of robust and scalable production methodologies, while collaborating closely with various...


  • Princeton, New Jersey, United States PMV Pharmaceuticals, Inc. Full time

    Lead Biostatistician in Oncology ResearchBecome a vital part of our forward-thinking team at PMV Pharmaceuticals, Inc., a leader in the development of innovative p53 reactivators aimed at revolutionizing cancer treatment. Our commitment to integrating biological insights with pharmaceutical advancements positions us at the cutting edge of cancer therapy.We...


  • Princeton, New Jersey, United States Cogentrix Full time

    Director- Risk ManagementCogentrix is seeking a seasoned professional to lead its risk management function, encompassing analysis, measurement, monitoring, and reporting of energy and commodity portfolio risks.Key Responsibilities:Develop and Implement Risk Reporting Frameworks: Design and implement effective risk reporting for all levels of commodity risk...


  • Princeton, New Jersey, United States Life Science People Full time

    The Director of Process Development will spearhead the advancement, refinement, and scaling of viral vector production within the organization. This position entails overseeing a team of process development professionals, ensuring the establishment of robust and scalable manufacturing protocols, and collaborating closely with various departments to fulfill...


  • Princeton, New Jersey, United States System One Holdings, LLC Full time

    Title: Clinical Safety Analytics Associate Company: System One Holdings, LLC Location: Hybrid Type: Contract Overview System One Holdings, LLC is seeking a Clinical Safety Analytics Associate to join our team. This role is essential within the Pharmacovigilance Center of Excellence (PV CoE). The Associate will focus on analyzing clinical and safety data to...


  • Princeton, New Jersey, United States Bristol-Myers Squibb Full time

    Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...


  • Princeton, New Jersey, United States Life Science People Full time

    The Director of Process Development will spearhead the advancement, refinement, and scaling of viral vector production within the organization. This pivotal role encompasses overseeing a team of scientists and engineers dedicated to process development, ensuring that production methods are both robust and scalable, while collaborating closely with various...