Bristol-Myers Squibb
Senior Manager, Biostatistics
Bristol-Myers Squibb, Princeton, New Jersey, us, 08543
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 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.
Employer:
Bristol-Myers Squibb CompanyJob Title:
Senior Manager, Biostatistics (ref.# 7928)Job Location:
3551 Lawrenceville Road, Princeton, NJ 08540
Duties:
Serve as a member of cross-functional development team and work on trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. Develop collaborative relationships and work effectively with the biostatistics lead and other cross functional team members. Collaborate in design of clinical study including methodology, data analysis and interpretation, and reporting of study results. Author and/or review protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, associated publications, and other study level specification documents. Perform and/or validate statistical analyses, advise ways to maximize clarity of data display. Communicate results to cross-functional teams, provides data interpretation in study documents such as clinical study reports, and publications. Translate scientific questions into statistical terms and statistical concepts into layman terms. Ensure compliance with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable. Develop technical knowledge of statistical methodology and how it is appropriately applied in trial design and data analysis for clear, concise, high-quality results. Continually enhance knowledge of drug development process, regulatory and commercial requirement. Develop and advise team members. May telecommute 100% of time to Princeton, NJ from any US location.
Requirements:
Doctorate degree in statistics, biostatistics or a related field plus the following knowledge/skills: SAS, R, WinBUGs/OpenBUGs. The knowledge/skills can be gained through education. Alternatively, master's degree in statistics, biostatistics or a related field plus 2 years of post-baccalaureate experience. Experience must include the following: SAS, R, WinBUGs/OpenBUGs.
Contact:
Althea WilsonBristol-Myers Squibb Company4931 George RoadTampa, FL 33634Resume.com@bms.com
The starting compensation for this job is a range from $143,915 to $194,708, plus incentive cash and stock opportunities (based on eligibility). The starting pay takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation is decided based on demonstrated experience.
Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as Transforming patients' lives through science, 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.
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 adastaffingsupport@bms.com.
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.
#J-18808-Ljbffr
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.
Employer:
Bristol-Myers Squibb CompanyJob Title:
Senior Manager, Biostatistics (ref.# 7928)Job Location:
3551 Lawrenceville Road, Princeton, NJ 08540
Duties:
Serve as a member of cross-functional development team and work on trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. Develop collaborative relationships and work effectively with the biostatistics lead and other cross functional team members. Collaborate in design of clinical study including methodology, data analysis and interpretation, and reporting of study results. Author and/or review protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, associated publications, and other study level specification documents. Perform and/or validate statistical analyses, advise ways to maximize clarity of data display. Communicate results to cross-functional teams, provides data interpretation in study documents such as clinical study reports, and publications. Translate scientific questions into statistical terms and statistical concepts into layman terms. Ensure compliance with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable. Develop technical knowledge of statistical methodology and how it is appropriately applied in trial design and data analysis for clear, concise, high-quality results. Continually enhance knowledge of drug development process, regulatory and commercial requirement. Develop and advise team members. May telecommute 100% of time to Princeton, NJ from any US location.
Requirements:
Doctorate degree in statistics, biostatistics or a related field plus the following knowledge/skills: SAS, R, WinBUGs/OpenBUGs. The knowledge/skills can be gained through education. Alternatively, master's degree in statistics, biostatistics or a related field plus 2 years of post-baccalaureate experience. Experience must include the following: SAS, R, WinBUGs/OpenBUGs.
Contact:
Althea WilsonBristol-Myers Squibb Company4931 George RoadTampa, FL 33634Resume.com@bms.com
The starting compensation for this job is a range from $143,915 to $194,708, plus incentive cash and stock opportunities (based on eligibility). The starting pay takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation is decided based on demonstrated experience.
Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as Transforming patients' lives through science, 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.
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 adastaffingsupport@bms.com.
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.
#J-18808-Ljbffr