Senior Manager (Data Scientist), Clinical Quality Analytics
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.
Read more:
careers.
bms.
com/working-with-us.
As a Senior Manager (Data Scientist), Clinical Quality Analytics, you will develop and deliver analyses of clinical trial and clinical trial quality (audits, inspections, deviations, etc.
) data to provide insights on the quality of BMS s innovative pipeline.
You will partner closely with clinical compliance, quality & risk management, data infrastructure, and process owners to ensure effective measures and analytics are in place and leveraged to enable a data driven approach to trial quality management.
You will carry out data analytics for Good Clinical Practice (GCP) quality to ensure a data driven approach is consistently applied to monitoring quality and compliance of business processes supporting trial operations.
You will execute against the clinical quality analytics plan(s), both near and long term.
You know how to analyze data to derive meaningful insights.
You participate in sharing objective performance and analytic results at relevant cross functional or within functional leadership quality reviews.
You will be a trusted partner enabling data driven decisions for clinical compliance and GCP quality and risk management.
If you are passionate about the intersection of metric & data analytics, we look forward to meeting you!Key Responsibilities Perform diagnostic, descriptive, predictive and prescriptive analytics to identify performance trends, root cause assessments and identify areas of continuous improvement Help define innovative trending and modelling techniques to analyze data, build insights and help drive innovative process improvements Be able to apply NLP techniques and understand how they can be leveraged to solve business problems Assist in creation of new mechanisms to monitor for quality signals using outputs from analytics, including descriptive analytics such as those from Tableau or Spotfire, and advanced analytics including signal detection, natural language processing, machine learning, and time-series analysis Apply analytical/statistical methods to complex and disparate data sources Develop and enhance clinical quality monitoring analysis tools, ensuring they meet key stakeholder needs Partner to implement analytic strategies and roadmap to optimally enable clinical quality and compliance and risk assessments Partner to drive insights, with a focus on quality metrics at global and regional levels, evaluating performance relative to industry peers and thresholds for action Actively participate in quality management initiatives, councils or reviews to deliver data driven insights and share key quality indicators that will predict risk or potential outcomes Help enable monthly, quarterly analytic reviews and deliver high-value analyses of trial quality according to needs of strategic and operational leaders Partner to ensure appropriate and timely development of predictive models of GCP quality, compliance and risk given needs of team leads in associated areas and data maturity Partner with team colleagues to proactively network and liaise with cross functional business stakeholders to identify, contextualize and deliver high value analytics and insights, while ensuring objectivity and consistency across the enterprise Participate in relevant strategic initiatives and process improvement initiatives to bring an explicit quality measurement framework to the performance of clinical trials Take part in annual clinical quality benchmarking programsKey Stakeholders Key stakeholders/clientso Director, Clinical Quality Analytics, Business Insights and Analytics R&Do Business Insights & Analytics leaders supporting governance teams o Business operations leaders or partners across key Clinical, R&D Quality, and Compliance functions Key matrix relationshipso Business Insights & Analytics teams supporting performance analytics o Global Developmento Research and Development Quality Qualifications &
Experience:
Minimum RequirementsDegree/Certification/Licensure University degree in scientific or technical field, preferably in a STEM field (e.
g.
Computer Science, other quantitative Sciences, Information/Data Science, Engineering, Mathematics/Statistics).
At least 3 years experience in data analytics, preferably in the pharmaceutical, medical devices, healthcare or related industry but other industry experience is also relevant Experience with building and deploying data science and data engineering solutions using established industry methods (MLOps, Git) to pharmaceutical related datasets is preferred Demonstrated ability to use data to drive decisions and answer key business questions Competencies:
Understanding of the application of advanced analytics, including predictive analytic modeling approaches related to structured and unstructured data is ideal Experience delivering in a matrix organization, including articulating value propositions, balancing a complex book of work while making trade-offs and managing demand Excellence in meeting facilitation and in both written and oral communication Demonstrated ability to build relationships (both virtual and in person) with senior stakeholders and peers, including ability to negotiate and manage stakeholder engagement Ability to be flexible and adapt quickly to the changing needs of the organization Have attention to detail, be highly organized and able to balance multiple tasks Have strong oral and written communication skills Have the ability to work individually and as part of a team Software that must be used independently and without assistance Programming experience in a modern data science language (Python or R) Experience with building data science and data engineering solutions strongly preferred.
Building/using business intelligence / data visualization tools such as Spotfire, Tableau, QLIK, etc.
Be proficient with Microsoft Office, Word, Excel (advanced proficiency) and Power PointBMS Behaviors Required Passion, Innovation, Accountability, Urgency, Integrity, inclusion #LI-Onsite #LI-HybridIf 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 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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.
Visit careers.
bms.
com/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.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
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:
careers.
bms.
com/working-with-us.
As a Senior Manager (Data Scientist), Clinical Quality Analytics, you will develop and deliver analyses of clinical trial and clinical trial quality (audits, inspections, deviations, etc.
) data to provide insights on the quality of BMS s innovative pipeline.
You will partner closely with clinical compliance, quality & risk management, data infrastructure, and process owners to ensure effective measures and analytics are in place and leveraged to enable a data driven approach to trial quality management.
You will carry out data analytics for Good Clinical Practice (GCP) quality to ensure a data driven approach is consistently applied to monitoring quality and compliance of business processes supporting trial operations.
You will execute against the clinical quality analytics plan(s), both near and long term.
You know how to analyze data to derive meaningful insights.
You participate in sharing objective performance and analytic results at relevant cross functional or within functional leadership quality reviews.
You will be a trusted partner enabling data driven decisions for clinical compliance and GCP quality and risk management.
If you are passionate about the intersection of metric & data analytics, we look forward to meeting you!Key Responsibilities Perform diagnostic, descriptive, predictive and prescriptive analytics to identify performance trends, root cause assessments and identify areas of continuous improvement Help define innovative trending and modelling techniques to analyze data, build insights and help drive innovative process improvements Be able to apply NLP techniques and understand how they can be leveraged to solve business problems Assist in creation of new mechanisms to monitor for quality signals using outputs from analytics, including descriptive analytics such as those from Tableau or Spotfire, and advanced analytics including signal detection, natural language processing, machine learning, and time-series analysis Apply analytical/statistical methods to complex and disparate data sources Develop and enhance clinical quality monitoring analysis tools, ensuring they meet key stakeholder needs Partner to implement analytic strategies and roadmap to optimally enable clinical quality and compliance and risk assessments Partner to drive insights, with a focus on quality metrics at global and regional levels, evaluating performance relative to industry peers and thresholds for action Actively participate in quality management initiatives, councils or reviews to deliver data driven insights and share key quality indicators that will predict risk or potential outcomes Help enable monthly, quarterly analytic reviews and deliver high-value analyses of trial quality according to needs of strategic and operational leaders Partner to ensure appropriate and timely development of predictive models of GCP quality, compliance and risk given needs of team leads in associated areas and data maturity Partner with team colleagues to proactively network and liaise with cross functional business stakeholders to identify, contextualize and deliver high value analytics and insights, while ensuring objectivity and consistency across the enterprise Participate in relevant strategic initiatives and process improvement initiatives to bring an explicit quality measurement framework to the performance of clinical trials Take part in annual clinical quality benchmarking programsKey Stakeholders Key stakeholders/clientso Director, Clinical Quality Analytics, Business Insights and Analytics R&Do Business Insights & Analytics leaders supporting governance teams o Business operations leaders or partners across key Clinical, R&D Quality, and Compliance functions Key matrix relationshipso Business Insights & Analytics teams supporting performance analytics o Global Developmento Research and Development Quality Qualifications &
Experience:
Minimum RequirementsDegree/Certification/Licensure University degree in scientific or technical field, preferably in a STEM field (e.
g.
Computer Science, other quantitative Sciences, Information/Data Science, Engineering, Mathematics/Statistics).
At least 3 years experience in data analytics, preferably in the pharmaceutical, medical devices, healthcare or related industry but other industry experience is also relevant Experience with building and deploying data science and data engineering solutions using established industry methods (MLOps, Git) to pharmaceutical related datasets is preferred Demonstrated ability to use data to drive decisions and answer key business questions Competencies:
Understanding of the application of advanced analytics, including predictive analytic modeling approaches related to structured and unstructured data is ideal Experience delivering in a matrix organization, including articulating value propositions, balancing a complex book of work while making trade-offs and managing demand Excellence in meeting facilitation and in both written and oral communication Demonstrated ability to build relationships (both virtual and in person) with senior stakeholders and peers, including ability to negotiate and manage stakeholder engagement Ability to be flexible and adapt quickly to the changing needs of the organization Have attention to detail, be highly organized and able to balance multiple tasks Have strong oral and written communication skills Have the ability to work individually and as part of a team Software that must be used independently and without assistance Programming experience in a modern data science language (Python or R) Experience with building data science and data engineering solutions strongly preferred.
Building/using business intelligence / data visualization tools such as Spotfire, Tableau, QLIK, etc.
Be proficient with Microsoft Office, Word, Excel (advanced proficiency) and Power PointBMS Behaviors Required Passion, Innovation, Accountability, Urgency, Integrity, inclusion #LI-Onsite #LI-HybridIf 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 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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.
Visit careers.
bms.
com/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.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
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