Senior Statistician / Principal Statistician
Bristol-Myers Squibb
Senior Statistician / Principal Statistician
Job Description
Apply statistical techniques to facilitate better decision-making and improve business operation. Regularly interact with management of different levels in strategy meetings. Contribute to strategic planning to ensure statistically optimized non-clinical development plans and assist in the creation of strategic objectives for regulatory filings. Provides leadership and statistical SME support for complex data analysis requests, including critical investigations, specification settings, stability analysis, and yield improvement initiatives. Takes accountability for ensuring quality and timely deliverables. Collaborates with global and site functions to identify areas for improvement in yield, robustness, and quality by applying statistical methods. Manages multiple studies to ensure consistency and adherence to standards within manufacturing and quality area Identify opportunities and drive innovation in advanced analytics and AI/ML techniques through process and quality applications. Act as a scientific and strategic partner to effectively engage with the matrix team in the drug manufacturing process and quality assurance. Connect and communicate with key stakeholders and the leadership team with statistical work in a clear, logical, complete, and transparent manner to support data-driven decisions. Prepare statistical courses and provide training to scientists. Mentor junior staff, proactively help with both their technical and career development, and seek general feedback and technical input from colleagues. Maintain awareness of external trends in advanced analytics and represent BMS at industry forums and conferences. Maintain and expand expertise in various computing tools to leverage internal and external data sets to drive decisions. Examples of such tools include R, Spotfire, SAS, etc. Continue development of various analysis tools to improve the process. Contributes to external and internal statistical community of practice. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Supporting People with Disabilities Senior Statistician: Bachelor's degree with 7+ years of experience or master's degree with 4+ years of experience or PhD with 2+ years of experience Principal Statistician: Bachelor's degree with 9+ years of experience or master's degree with 7+ years of experience or PhD with 4+ years of experience in Statistics or a related field. High degree of technical competence and excellent communication skills, both oral and written Able to manage project timeline and quality of deliverables Able to build strong relationship with peers and cross-functional partners to achieve higher performance. Highly motivated to drive innovation by raising the bar and challenging the status quo Have strong leadership skills and experience in working/managing a team. Pharmaceutical or related industry knowledge required, including experience and understanding of drug development and life-cycle management in the regulated environment. Experience in a cGMP-regulated environment, preferably gained through direct support of commercial manufacturing. Extensive knowledge of FDA/EMEA cGMPs and other global regulatory compliance guidelines (e.g., ICH) for drug manufacturing, packaging, and distribution. Proficiency in scientific computing/programming/software (SAS, R or Python, JMP) and implementation of advanced statistical analysis, data manipulation, graphing & simulation.
About the Role/Company
- BMS is involved in the pharmaceutical industry
- The company values innovation and data-driven decision-making
- BMS supports participation in industry forums and conferences
Key Responsibilities
- Apply statistical techniques to facilitate better decision-making and improve business operations
- Regularly interact with management of different levels in strategy meetings
- Contribute to strategic planning to ensure statistically optimized non-clinical development plans
- Assist in the creation of strategic objectives for regulatory filings
- Provide leadership and statistical SME support for complex data analysis requests, including critical investigations, specification settings, stability analysis, and yield improvement initiatives
- Take accountability for ensuring quality and timely deliverables
- Collaborate with global and site functions to identify areas for improvement in yield, robustness, and quality by applying statistical methods
- Manage multiple studies to ensure consistency and adherence to standards within manufacturing and quality areas
- Identify opportunities and drive innovation in advanced analytics and AI/ML techniques through process and quality applications
- Act as a scientific and strategic partner to effectively engage with the matrix team in the drug manufacturing process and quality assurance
- Connect and communicate with key stakeholders and the leadership team with statistical work in a clear, logical, complete, and transparent manner to support data-driven decisions
- Prepare statistical courses and provide training to scientists
- Mentor junior staff, proactively help with both their technical and career development, and seek general feedback and technical input from colleagues
- Maintain awareness of external trends in advanced analytics and represent BMS at industry forums and conferences
- Maintain and expand expertise in various computing tools to leverage internal and external data sets to drive decisions
- Continue development of various analysis tools to improve the process
- Contribute to external and internal statistical community of practice
Required Qualifications
- Bachelor's degree with 7+ years of experience or master's degree with 4+ years of experience or PhD with 2+ years of experience for Senior Statistician
- Bachelor's degree with 9+ years of experience or master's degree with 7+ years of experience or PhD with 4+ years of experience for Principal Statistician
- Degree in Statistics or a related field
Preferred Qualifications
- Experience in a cGMP-regulated environment, preferably gained through direct support of commercial manufacturing
- Extensive knowledge of FDA/EMEA cGMPs and other global regulatory compliance guidelines (e.g., ICH) for drug manufacturing, packaging, and distribution
Skills Required
- High degree of technical competence
- Excellent communication skills, both oral and written
- Ability to manage project timeline and quality of deliverables
- Ability to build strong relationships with peers and cross-functional partners to achieve higher performance
- Highly motivated to drive innovation by raising the bar and challenging the status quo
- Strong leadership skills and experience in working/managing a team
- Pharmaceutical or related industry knowledge, including experience and understanding of drug development and life-cycle management in the regulated environment
- Proficiency in scientific computing/programming/software (SAS, R or Python, JMP) and implementation of advanced statistical analysis, data manipulation, graphing & simulation
Benefits & Perks
- Paid national holidays and optional holidays
- Global Shutdown Days between Christmas and New Year's holiday
- Up to 120 hours of paid vacation
- Up to two (2) paid days to volunteer
- Sick time off
- Summer hours flexibility
- Support for people with disabilities
Locations
- Devens MA, United States
- Cruiserath, IE
- New Brunswick NJ, United States
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
120,000 - 180,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- High degree of technical competenceintermediate
- Excellent communication skills, both oral and writtenintermediate
- Ability to manage project timeline and quality of deliverablesintermediate
- Ability to build strong relationships with peers and cross-functional partners to achieve higher performanceintermediate
- Highly motivated to drive innovation by raising the bar and challenging the status quointermediate
- Strong leadership skills and experience in working/managing a teamintermediate
- Pharmaceutical or related industry knowledge, including experience and understanding of drug development and life-cycle management in the regulated environmentintermediate
- Proficiency in scientific computing/programming/software (SAS, R or Python, JMP) and implementation of advanced statistical analysis, data manipulation, graphing & simulationintermediate
Required Qualifications
- Bachelor's degree with 7+ years of experience or master's degree with 4+ years of experience or PhD with 2+ years of experience for Senior Statistician (experience)
- Bachelor's degree with 9+ years of experience or master's degree with 7+ years of experience or PhD with 4+ years of experience for Principal Statistician (experience)
- Degree in Statistics or a related field (experience)
Preferred Qualifications
- Experience in a cGMP-regulated environment, preferably gained through direct support of commercial manufacturing (experience)
- Extensive knowledge of FDA/EMEA cGMPs and other global regulatory compliance guidelines (e.g., ICH) for drug manufacturing, packaging, and distribution (experience)
Responsibilities
- Apply statistical techniques to facilitate better decision-making and improve business operations
- Regularly interact with management of different levels in strategy meetings
- Contribute to strategic planning to ensure statistically optimized non-clinical development plans
- Assist in the creation of strategic objectives for regulatory filings
- Provide leadership and statistical SME support for complex data analysis requests, including critical investigations, specification settings, stability analysis, and yield improvement initiatives
- Take accountability for ensuring quality and timely deliverables
- Collaborate with global and site functions to identify areas for improvement in yield, robustness, and quality by applying statistical methods
- Manage multiple studies to ensure consistency and adherence to standards within manufacturing and quality areas
- Identify opportunities and drive innovation in advanced analytics and AI/ML techniques through process and quality applications
- Act as a scientific and strategic partner to effectively engage with the matrix team in the drug manufacturing process and quality assurance
- Connect and communicate with key stakeholders and the leadership team with statistical work in a clear, logical, complete, and transparent manner to support data-driven decisions
- Prepare statistical courses and provide training to scientists
- Mentor junior staff, proactively help with both their technical and career development, and seek general feedback and technical input from colleagues
- Maintain awareness of external trends in advanced analytics and represent BMS at industry forums and conferences
- Maintain and expand expertise in various computing tools to leverage internal and external data sets to drive decisions
- Continue development of various analysis tools to improve the process
- Contribute to external and internal statistical community of practice
Benefits
- general: Paid national holidays and optional holidays
- general: Global Shutdown Days between Christmas and New Year's holiday
- general: Up to 120 hours of paid vacation
- general: Up to two (2) paid days to volunteer
- general: Sick time off
- general: Summer hours flexibility
- general: Support for people with disabilities
Tags & Categories
Senior Statistician / Principal Statistician
Bristol-Myers Squibb
Senior Statistician / Principal Statistician
Job Description
Apply statistical techniques to facilitate better decision-making and improve business operation. Regularly interact with management of different levels in strategy meetings. Contribute to strategic planning to ensure statistically optimized non-clinical development plans and assist in the creation of strategic objectives for regulatory filings. Provides leadership and statistical SME support for complex data analysis requests, including critical investigations, specification settings, stability analysis, and yield improvement initiatives. Takes accountability for ensuring quality and timely deliverables. Collaborates with global and site functions to identify areas for improvement in yield, robustness, and quality by applying statistical methods. Manages multiple studies to ensure consistency and adherence to standards within manufacturing and quality area Identify opportunities and drive innovation in advanced analytics and AI/ML techniques through process and quality applications. Act as a scientific and strategic partner to effectively engage with the matrix team in the drug manufacturing process and quality assurance. Connect and communicate with key stakeholders and the leadership team with statistical work in a clear, logical, complete, and transparent manner to support data-driven decisions. Prepare statistical courses and provide training to scientists. Mentor junior staff, proactively help with both their technical and career development, and seek general feedback and technical input from colleagues. Maintain awareness of external trends in advanced analytics and represent BMS at industry forums and conferences. Maintain and expand expertise in various computing tools to leverage internal and external data sets to drive decisions. Examples of such tools include R, Spotfire, SAS, etc. Continue development of various analysis tools to improve the process. Contributes to external and internal statistical community of practice. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Supporting People with Disabilities Senior Statistician: Bachelor's degree with 7+ years of experience or master's degree with 4+ years of experience or PhD with 2+ years of experience Principal Statistician: Bachelor's degree with 9+ years of experience or master's degree with 7+ years of experience or PhD with 4+ years of experience in Statistics or a related field. High degree of technical competence and excellent communication skills, both oral and written Able to manage project timeline and quality of deliverables Able to build strong relationship with peers and cross-functional partners to achieve higher performance. Highly motivated to drive innovation by raising the bar and challenging the status quo Have strong leadership skills and experience in working/managing a team. Pharmaceutical or related industry knowledge required, including experience and understanding of drug development and life-cycle management in the regulated environment. Experience in a cGMP-regulated environment, preferably gained through direct support of commercial manufacturing. Extensive knowledge of FDA/EMEA cGMPs and other global regulatory compliance guidelines (e.g., ICH) for drug manufacturing, packaging, and distribution. Proficiency in scientific computing/programming/software (SAS, R or Python, JMP) and implementation of advanced statistical analysis, data manipulation, graphing & simulation.
About the Role/Company
- BMS is involved in the pharmaceutical industry
- The company values innovation and data-driven decision-making
- BMS supports participation in industry forums and conferences
Key Responsibilities
- Apply statistical techniques to facilitate better decision-making and improve business operations
- Regularly interact with management of different levels in strategy meetings
- Contribute to strategic planning to ensure statistically optimized non-clinical development plans
- Assist in the creation of strategic objectives for regulatory filings
- Provide leadership and statistical SME support for complex data analysis requests, including critical investigations, specification settings, stability analysis, and yield improvement initiatives
- Take accountability for ensuring quality and timely deliverables
- Collaborate with global and site functions to identify areas for improvement in yield, robustness, and quality by applying statistical methods
- Manage multiple studies to ensure consistency and adherence to standards within manufacturing and quality areas
- Identify opportunities and drive innovation in advanced analytics and AI/ML techniques through process and quality applications
- Act as a scientific and strategic partner to effectively engage with the matrix team in the drug manufacturing process and quality assurance
- Connect and communicate with key stakeholders and the leadership team with statistical work in a clear, logical, complete, and transparent manner to support data-driven decisions
- Prepare statistical courses and provide training to scientists
- Mentor junior staff, proactively help with both their technical and career development, and seek general feedback and technical input from colleagues
- Maintain awareness of external trends in advanced analytics and represent BMS at industry forums and conferences
- Maintain and expand expertise in various computing tools to leverage internal and external data sets to drive decisions
- Continue development of various analysis tools to improve the process
- Contribute to external and internal statistical community of practice
Required Qualifications
- Bachelor's degree with 7+ years of experience or master's degree with 4+ years of experience or PhD with 2+ years of experience for Senior Statistician
- Bachelor's degree with 9+ years of experience or master's degree with 7+ years of experience or PhD with 4+ years of experience for Principal Statistician
- Degree in Statistics or a related field
Preferred Qualifications
- Experience in a cGMP-regulated environment, preferably gained through direct support of commercial manufacturing
- Extensive knowledge of FDA/EMEA cGMPs and other global regulatory compliance guidelines (e.g., ICH) for drug manufacturing, packaging, and distribution
Skills Required
- High degree of technical competence
- Excellent communication skills, both oral and written
- Ability to manage project timeline and quality of deliverables
- Ability to build strong relationships with peers and cross-functional partners to achieve higher performance
- Highly motivated to drive innovation by raising the bar and challenging the status quo
- Strong leadership skills and experience in working/managing a team
- Pharmaceutical or related industry knowledge, including experience and understanding of drug development and life-cycle management in the regulated environment
- Proficiency in scientific computing/programming/software (SAS, R or Python, JMP) and implementation of advanced statistical analysis, data manipulation, graphing & simulation
Benefits & Perks
- Paid national holidays and optional holidays
- Global Shutdown Days between Christmas and New Year's holiday
- Up to 120 hours of paid vacation
- Up to two (2) paid days to volunteer
- Sick time off
- Summer hours flexibility
- Support for people with disabilities
Locations
- Devens MA, United States
- Cruiserath, IE
- New Brunswick NJ, United States
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
120,000 - 180,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- High degree of technical competenceintermediate
- Excellent communication skills, both oral and writtenintermediate
- Ability to manage project timeline and quality of deliverablesintermediate
- Ability to build strong relationships with peers and cross-functional partners to achieve higher performanceintermediate
- Highly motivated to drive innovation by raising the bar and challenging the status quointermediate
- Strong leadership skills and experience in working/managing a teamintermediate
- Pharmaceutical or related industry knowledge, including experience and understanding of drug development and life-cycle management in the regulated environmentintermediate
- Proficiency in scientific computing/programming/software (SAS, R or Python, JMP) and implementation of advanced statistical analysis, data manipulation, graphing & simulationintermediate
Required Qualifications
- Bachelor's degree with 7+ years of experience or master's degree with 4+ years of experience or PhD with 2+ years of experience for Senior Statistician (experience)
- Bachelor's degree with 9+ years of experience or master's degree with 7+ years of experience or PhD with 4+ years of experience for Principal Statistician (experience)
- Degree in Statistics or a related field (experience)
Preferred Qualifications
- Experience in a cGMP-regulated environment, preferably gained through direct support of commercial manufacturing (experience)
- Extensive knowledge of FDA/EMEA cGMPs and other global regulatory compliance guidelines (e.g., ICH) for drug manufacturing, packaging, and distribution (experience)
Responsibilities
- Apply statistical techniques to facilitate better decision-making and improve business operations
- Regularly interact with management of different levels in strategy meetings
- Contribute to strategic planning to ensure statistically optimized non-clinical development plans
- Assist in the creation of strategic objectives for regulatory filings
- Provide leadership and statistical SME support for complex data analysis requests, including critical investigations, specification settings, stability analysis, and yield improvement initiatives
- Take accountability for ensuring quality and timely deliverables
- Collaborate with global and site functions to identify areas for improvement in yield, robustness, and quality by applying statistical methods
- Manage multiple studies to ensure consistency and adherence to standards within manufacturing and quality areas
- Identify opportunities and drive innovation in advanced analytics and AI/ML techniques through process and quality applications
- Act as a scientific and strategic partner to effectively engage with the matrix team in the drug manufacturing process and quality assurance
- Connect and communicate with key stakeholders and the leadership team with statistical work in a clear, logical, complete, and transparent manner to support data-driven decisions
- Prepare statistical courses and provide training to scientists
- Mentor junior staff, proactively help with both their technical and career development, and seek general feedback and technical input from colleagues
- Maintain awareness of external trends in advanced analytics and represent BMS at industry forums and conferences
- Maintain and expand expertise in various computing tools to leverage internal and external data sets to drive decisions
- Continue development of various analysis tools to improve the process
- Contribute to external and internal statistical community of practice
Benefits
- general: Paid national holidays and optional holidays
- general: Global Shutdown Days between Christmas and New Year's holiday
- general: Up to 120 hours of paid vacation
- general: Up to two (2) paid days to volunteer
- general: Sick time off
- general: Summer hours flexibility
- general: Support for people with disabilities
Tags & Categories