Senior Director, Risk Diligence and Oversight - Bristol Myers Squibb
Princeton, NJ
About the Job
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: careers.bms.com/working-with-us .
Summary:
The Senior Director of Risk Diligence and Oversight will play a critical leadership role in managing and overseeing third party risk for Bristol Myers Squibb. This position focuses on healthcare compliance diligence and the oversight of all third-party relationships across all risk domains. The ideal candidate will possess extensive experience in risk management, healthcare compliance, and third-party oversight, with a strategic mindset and the ability to influence and collaborate with senior stakeholders across the organization.
Key Responsibilities:
Healthcare Compliance Risk Diligence and Oversight:
+ Lead and manage comprehensive healthcare compliance third party diligence processes to ensure adherence to regulatory requirements and internal standards.
+ Collaborate with market compliance professionals and other internal stakeholders to identify and assess compliance risks associated with third-party engagements.
+ Provide strategic advisory support on third-party healthcare compliance matters to senior leadership and business units.
+ Develop and maintain risk assessment models, inputs, and requirements.
+ Partner with risk owners and business stakeholders to conduct risk assessments and provide training on risk management best practices.
+ Facilitate risk assessment calibration and stratification processes to ensure consistency and accuracy.
+ Report risk assessment findings and insights to senior leadership and designated stakeholders, providing clear and actionable recommendations.
Third-Party Oversight:
+ Deliver comprehensive insights on risks for all third-party relationships across all risk domains, including financial, operational, compliance, reputational, and strategic risks.
+ Inform and maintain third-party risk management policies, procedures, and tools.
+ Monitor and review the performance and risk exposure of existing third-party relationships, ensuring ongoing compliance and risk mitigation.
Strategic Leadership:
+ Provide strategic direction and leadership to the third party risk diligence and oversight function, aligning with the company's overall risk management strategy.
+ Collaborate with cross-functional teams to integrate risk management practices into business processes and decision-making.
+ Drive continuous improvement in risk diligence and oversight practices, leveraging industry best practices and emerging trends.
+ Represent the company in external forums and industry groups related to risk management and compliance.
Qualifications & Experience:
+ Bachelor's degree in Risk Management, Business Administration, Finance, Law, or a related field; advanced degree (MBA, JD, etc.) preferred.
+ Minimum of 12-15 years of experience in risk management, healthcare compliance, or a related field, with significant experience in a senior leadership role, preferably within the biopharmaceutical industry.
+ Deep understanding of healthcare compliance regulations, third-party risk management, and risk assessment methodologies.
+ Proven experience in and implementing third party risk diligence and oversight frameworks and tools.
+ Exceptional analytical and problem-solving skills, with the ability to interpret complex data and develop strategic insights.
+ Strong communication and interpersonal skills, with the ability to effectively influence and collaborate with senior stakeholders at all levels of the organization.
+ Experience in conducting training and providing strategic advisory support to senior risk owners and business stakeholders.
+ Ability to manage multiple high-priority projects and initiatives in a fast-paced, dynamic environment.
+ Proficiency in advanced risk management software and tools.
+ Strong attention to detail and commitment to maintaining high standards of quality and accuracy.
+ Demonstrated ability to think strategically and drive organizational change.
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 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:
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 adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) 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.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Company: Bristol-Myers Squibb
Req Number: R1585277
Updated: 2025-01-03 05:01:27.933 UTC
Location: Princeton-NJ
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
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: careers.bms.com/working-with-us .
Summary:
The Senior Director of Risk Diligence and Oversight will play a critical leadership role in managing and overseeing third party risk for Bristol Myers Squibb. This position focuses on healthcare compliance diligence and the oversight of all third-party relationships across all risk domains. The ideal candidate will possess extensive experience in risk management, healthcare compliance, and third-party oversight, with a strategic mindset and the ability to influence and collaborate with senior stakeholders across the organization.
Key Responsibilities:
Healthcare Compliance Risk Diligence and Oversight:
+ Lead and manage comprehensive healthcare compliance third party diligence processes to ensure adherence to regulatory requirements and internal standards.
+ Collaborate with market compliance professionals and other internal stakeholders to identify and assess compliance risks associated with third-party engagements.
+ Provide strategic advisory support on third-party healthcare compliance matters to senior leadership and business units.
+ Develop and maintain risk assessment models, inputs, and requirements.
+ Partner with risk owners and business stakeholders to conduct risk assessments and provide training on risk management best practices.
+ Facilitate risk assessment calibration and stratification processes to ensure consistency and accuracy.
+ Report risk assessment findings and insights to senior leadership and designated stakeholders, providing clear and actionable recommendations.
Third-Party Oversight:
+ Deliver comprehensive insights on risks for all third-party relationships across all risk domains, including financial, operational, compliance, reputational, and strategic risks.
+ Inform and maintain third-party risk management policies, procedures, and tools.
+ Monitor and review the performance and risk exposure of existing third-party relationships, ensuring ongoing compliance and risk mitigation.
Strategic Leadership:
+ Provide strategic direction and leadership to the third party risk diligence and oversight function, aligning with the company's overall risk management strategy.
+ Collaborate with cross-functional teams to integrate risk management practices into business processes and decision-making.
+ Drive continuous improvement in risk diligence and oversight practices, leveraging industry best practices and emerging trends.
+ Represent the company in external forums and industry groups related to risk management and compliance.
Qualifications & Experience:
+ Bachelor's degree in Risk Management, Business Administration, Finance, Law, or a related field; advanced degree (MBA, JD, etc.) preferred.
+ Minimum of 12-15 years of experience in risk management, healthcare compliance, or a related field, with significant experience in a senior leadership role, preferably within the biopharmaceutical industry.
+ Deep understanding of healthcare compliance regulations, third-party risk management, and risk assessment methodologies.
+ Proven experience in and implementing third party risk diligence and oversight frameworks and tools.
+ Exceptional analytical and problem-solving skills, with the ability to interpret complex data and develop strategic insights.
+ Strong communication and interpersonal skills, with the ability to effectively influence and collaborate with senior stakeholders at all levels of the organization.
+ Experience in conducting training and providing strategic advisory support to senior risk owners and business stakeholders.
+ Ability to manage multiple high-priority projects and initiatives in a fast-paced, dynamic environment.
+ Proficiency in advanced risk management software and tools.
+ Strong attention to detail and commitment to maintaining high standards of quality and accuracy.
+ Demonstrated ability to think strategically and drive organizational change.
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 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:
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 adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) 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.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Company: Bristol-Myers Squibb
Req Number: R1585277
Updated: 2025-01-03 05:01:27.933 UTC
Location: Princeton-NJ
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Source : Bristol Myers Squibb