Auf einen Blick
- Aufgaben: Leitung des Compliance & Ethics Programms, Entwicklung und Implementierung von Richtlinien und Schulungen.
- Arbeitgeber: Bristol Myers Squibb, ein Unternehmen, das durch Wissenschaft Patientenleben transformiert.
- Mitarbeitervorteile: Flexible Arbeitsmodelle, umfangreiche Mitarbeiterbenefits und -services.
- Warum dieser Job: Einflussreiche Position in einem global agierenden Unternehmen mit starkem Fokus auf Diversität und Innovation.
- Gewünschte Qualifikationen: Bachelor erforderlich, vorzugsweise höherer Abschluss, 8+ Jahre Erfahrung in Compliance oder Recht im Pharma-/Gesundheitsbereich.
- Andere Informationen: Hybrid-Arbeitsmodell mit mindestens 50% Präsenz am Standort.
Das voraussichtliche Gehalt liegt zwischen 100000 - 140000 € pro Jahr.
Job Information
Bristol Myers Squibb Director of Compliance & Ethics, Germany (m/w/d) in Munich, Germany
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 Vice President, European Markets & Japan Compliance and Ethics, this role partners with the market’s executive leadership team as well as senior leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory, IT, Audit, Finance and HR to ensure continuous improvement and enhancements to the BMS Germany C&E program. The Director of Compliance will work cross-functionally at all levels of the organization to embed Compliance & Ethics policies and principles into market business initiatives to ensure operations are compliant-by-design.
The role requires subject matter expertise in German and applicable EU laws, regulations and codes governing pharmaceutical manufacturer’s interactions and engagements with German healthcare professionals, healthcare organizations, patients, patient advocacy organizations and government officials. In addition, substantive knowledge and experience implementing compliance risk mitigation strategies, such as education and monitoring, with data analytics and executional risk to help the business make well-informed, risk-based decisions.
Responsibilities Include:
- Develop and execute a comprehensive annual compliance work plan for BMS Germany responsive to new business strategies, initiatives and ongoing market operations.
- Сo-Chair (with the General Manager) BMS Germany’s Compliance Committee.
- Promote the right tone throughout the organization and, working with the leadership team, ensure a steadfast commitment by all employees to integrity and compliance.
- Partner and create synergy with the market’s Regulatory Law team to provide high quality service and guidance to the market’s business teams and other enabling functions.
- Drive German market implementation of BMS Global Compliance and Ethics program initiatives.
- Develop and deliver local market compliance policies, education and strategic communications. Ensure the market has a robust compliance monitoring program in place to timely and accurately identify compliance risk exposures. Conduct live or transactional monitoring of business activities. Review data to identify outliers and implement preventive measures or corrective action.
- Ensure compliance implementation, when applicable, of global SOPs, education, training/strategic communications, and monitoring & analytics in close cooperation with the global C&E Organization.
- Design and lead the periodic compliance risk assessment for Germany.
- Support scoping of BMS Germany internal audits by collaborating with the Global Internal Audit team.
- Partner with the third-party due diligence center of excellence on assessments of third parties operating in the market. Partner with the market business controls function team on ongoing management of market third parties with a healthcare compliance risk exposure.
- Establish a network of Compliance Champions in BMS Germany to integrate compliance messaging and concepts into established business training cycles. Identify and leverage key stakeholders and cross-functional resources to create buy-in for integrity and compliance culture initiatives across the market.
- Maintain working knowledge of local industry codes and regulations as well as government enforcement actions to identify and mitigate potential compliance risks.
- Perform other compliance-related activities as directed by the Chief Compliance & Ethics Officer, the VP, European Markets & Japan C&E or the Global Compliance & Ethics Leadership Team.
Qualifications:
- Bachelor’s Degree required. Advanced degree strongly preferred.
- 8+ year’s pharmaceutical or healthcare related compliance or legal experience, with at least 5 years-experience directly advising clients.
- Expert knowledge of relevant German and EU pharmaceutical compliance laws, regulations, codes and binding/non-binding guidance.
- Expert knowledge of the roles and responsibilities of commercial sales, marketing, medical affairs, and market access organizations in the pharmaceutical industry.
- Ability to influence and partner with senior level executives. Work from an enterprise mindset focused on achieving company goals in a compliant and ethical manner.
- Demonstrated ability to influence business decisions across all levels of the organization.
- Comfort with using data to tell stories particularly around risk and effectiveness of risk mitigation strategies.
- 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 HCPs/HCOs or patient advocacy organizations.
#LI-Hybrid
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.
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: R1583951
Updated: 2024-08-23 02:49:23.413 UTC
Location: Munich-DE
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.
Apply Now
Director of Compliance & Ethics, Germany (m/w/d) Arbeitgeber: Bristol-Myers Squibb GmbH & Co. KGaA
Kontaktperson:
Bristol-Myers Squibb GmbH & Co. KGaA HR Team
adastaffingsupport@bms.com