Associate Director, Compliance and Ethics Organization - Worldwide Medical, R&D and Global Drug Development - 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 .
Position Summary :
Reporting to the Senior Direc t o r , US and Above Market Medical and Market Access C&E Lead , this role partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory, IT, Audit, Finance and HR to build and integrate one global compliance program into the Worldwide Medical, R&D and Global Drug Development Organizations . In this role, you will combine your knowledge about risk mitigation strategies , such as education and monitoring, with data analytics about executional risk to help the business make well-informed, risk-based decisions . You will help operationalize those decisions by crafting simple, clear, principle-based policies . You will educate the business about those policies - and why they exist - leveraging adult-learning techniques that aid retention . And you will use a combination of live monitoring, transactional monitoring, and data analytics to monitor the business's adherence to those policies, helping the business remediate deviations from policies by identifying and addressing the root causes of those deviations . The ideal candidate will be able to execute these tasks with a mindset that believes business functions and Compliance and Ethics are equally accountable for both company success and ethical behavior and will be recognized internally and externally as an expert in mitigating healthcare compliance risk through providing advice, drafting policy, providing education and monitoring execution of high-risk activities.
Responsibilities Include :
+ Conduct risk assessments specific to medical affairs and clinical trial /research activities, utilizing a combination of data analytics, external and internal benchmarking , and review of enforcement trends, to proactively identify the most pressing areas of risk.
+ Foster trusting relationship with business leaders that enable you to learn of - and advise on - executional risk associated with new initiatives and counsel business leaders about educational initiatives, new policies or monitoring capabilities that can help mitigate risk associated with their decisions .
+ Analyze data regarding execution of analogous activities to better inform business leaders of the risk associated with their decisions.
+ Under the direction of the Senior Director, US and Above Market Medical and Market Access C&E Lead, d raft simple, easy to understand policies specific to medical affairs and clinical trial/research activities that empower the business to execute activities in an ethical and efficient way.
+ Under the direction of the Senior Director, US and Above Market Medical and Market Access C&E Lead, d evelop and provide training specific to medical affairs and clinical trial/research activities that utilizes adult-learning principles, such as gaming, microlearning, and experiential learning, to enhance retention of compliance messages.
+ Establish a network of Compliance C hampions in the respective business unit to integrate compliance messaging and concepts into established business training cycles .
+ Develop a framework for conducting live and transactional monitoring of medical affairs and clinical trial/research activities .
+ Review data to identify outliers and implement preventive education or additional monitoring in response .
+ Perform other compliance-related activities as directed by the Global Compliance & Ethics team and/or the Head of US and Above Market Compliance .
Qualifications :
+ Bachelor's degree .
+ Advanced degree (MBA, CPA, JD) appreciated but not required .
+ 8-12 years pharmaceutical or healthcare related compliance or legal experience.
+ Working knowledge of relevant pharmaceutical compliance guidelines, regulations (AKS, FCA, FDCA, HIPAA, FCPA) and PhRMA Code principles.
+ Familiarity with healthcare compliance risks associated with clinical trial placement and recruitmen t , advisory boards , medical congresses and other research and development or medical affairs activities.
+ Familiarity with practices of and intersections between commercial sales, marketing, and medical affairs organizations in the pharmaceutical industry a plus.
+ Ability to work and communicate with senior level executives with an enterprise mindset focused on achieving company goals in a compliant and ethical manner.
+ Demonstrated ability to influence business decisions.
+ Comfort with using data to tell stories particularly around risk and effectiveness of risk mitigation strategies.
+ Entrepreneurial spirit, taking ownership over the risks and processes you identify and searching for creative solutions.
+ Proven experience drafting principle-based policies.
+ Experience utilizing adult-learning concepts in corporate educational and training materials.
+ Experience conducting live monitoring of speaker programs and advisory boards, and transactional monitoring of engagements with health care providers.
+ Commitment to a diverse and inclusive workplace.
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: R1583123
Updated: 2024-10-04 03:11:07.928 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 .
Position Summary :
Reporting to the Senior Direc t o r , US and Above Market Medical and Market Access C&E Lead , this role partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory, IT, Audit, Finance and HR to build and integrate one global compliance program into the Worldwide Medical, R&D and Global Drug Development Organizations . In this role, you will combine your knowledge about risk mitigation strategies , such as education and monitoring, with data analytics about executional risk to help the business make well-informed, risk-based decisions . You will help operationalize those decisions by crafting simple, clear, principle-based policies . You will educate the business about those policies - and why they exist - leveraging adult-learning techniques that aid retention . And you will use a combination of live monitoring, transactional monitoring, and data analytics to monitor the business's adherence to those policies, helping the business remediate deviations from policies by identifying and addressing the root causes of those deviations . The ideal candidate will be able to execute these tasks with a mindset that believes business functions and Compliance and Ethics are equally accountable for both company success and ethical behavior and will be recognized internally and externally as an expert in mitigating healthcare compliance risk through providing advice, drafting policy, providing education and monitoring execution of high-risk activities.
Responsibilities Include :
+ Conduct risk assessments specific to medical affairs and clinical trial /research activities, utilizing a combination of data analytics, external and internal benchmarking , and review of enforcement trends, to proactively identify the most pressing areas of risk.
+ Foster trusting relationship with business leaders that enable you to learn of - and advise on - executional risk associated with new initiatives and counsel business leaders about educational initiatives, new policies or monitoring capabilities that can help mitigate risk associated with their decisions .
+ Analyze data regarding execution of analogous activities to better inform business leaders of the risk associated with their decisions.
+ Under the direction of the Senior Director, US and Above Market Medical and Market Access C&E Lead, d raft simple, easy to understand policies specific to medical affairs and clinical trial/research activities that empower the business to execute activities in an ethical and efficient way.
+ Under the direction of the Senior Director, US and Above Market Medical and Market Access C&E Lead, d evelop and provide training specific to medical affairs and clinical trial/research activities that utilizes adult-learning principles, such as gaming, microlearning, and experiential learning, to enhance retention of compliance messages.
+ Establish a network of Compliance C hampions in the respective business unit to integrate compliance messaging and concepts into established business training cycles .
+ Develop a framework for conducting live and transactional monitoring of medical affairs and clinical trial/research activities .
+ Review data to identify outliers and implement preventive education or additional monitoring in response .
+ Perform other compliance-related activities as directed by the Global Compliance & Ethics team and/or the Head of US and Above Market Compliance .
Qualifications :
+ Bachelor's degree .
+ Advanced degree (MBA, CPA, JD) appreciated but not required .
+ 8-12 years pharmaceutical or healthcare related compliance or legal experience.
+ Working knowledge of relevant pharmaceutical compliance guidelines, regulations (AKS, FCA, FDCA, HIPAA, FCPA) and PhRMA Code principles.
+ Familiarity with healthcare compliance risks associated with clinical trial placement and recruitmen t , advisory boards , medical congresses and other research and development or medical affairs activities.
+ Familiarity with practices of and intersections between commercial sales, marketing, and medical affairs organizations in the pharmaceutical industry a plus.
+ Ability to work and communicate with senior level executives with an enterprise mindset focused on achieving company goals in a compliant and ethical manner.
+ Demonstrated ability to influence business decisions.
+ Comfort with using data to tell stories particularly around risk and effectiveness of risk mitigation strategies.
+ Entrepreneurial spirit, taking ownership over the risks and processes you identify and searching for creative solutions.
+ Proven experience drafting principle-based policies.
+ Experience utilizing adult-learning concepts in corporate educational and training materials.
+ Experience conducting live monitoring of speaker programs and advisory boards, and transactional monitoring of engagements with health care providers.
+ Commitment to a diverse and inclusive workplace.
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: R1583123
Updated: 2024-10-04 03:11:07.928 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