Compliance Director UK/Ireland

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. Bristol Myers Squibb recognises the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programmes that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Position Summary

This is an above-market role with 60% support for the UK/Affiliate and 40% support for live field and transactional monitoring and global compliance risk assessments across the Europe Region. Responsible for leading Compliance & Ethics operations in UK/Ireland and effectively promoting the culture of integrity in the affiliate. Partner with stakeholders across the affiliate (including the Code Governance team) and serve as a member of the affiliate’s leadership team. Responsible for conducting live field and transactional monitoring across the Europe Region, with a focus on cross-border engagements and other moderate to high-risk exposure activities.

Key Responsibilities

• UK/Affiliate Responsibilities

• Develop and execute a comprehensive annual compliance work plan for the United Kingdom and Ireland responsive to new business strategies, initiatives and ongoing market operations.
• Co-Chair the Compliance Committee with the affiliate’s General Managers.
• Promote the right tone throughout the organization and, working with the Code Governance team and the affiliate leadership team, ensure a steadfast commitment by all employees to integrity, quality, compliance, and uncompromising ethics.
• Partner and create synergy with the affiliate Regulatory Law team to provide high quality advice and service to the market business operations.
• Drive local market implementation of BMS Global Compliance and Ethics program initiatives.
• Develop and implement new product/indication compliance assurance roadmap for launches in the UK/IE affiliate.
• Ensure compliance oversight for certain procedures, education, training/strategic communications, and monitoring & analytics in close cooperation with the Code Governance team and the global C&E Organization.
• Lead the affiliate’s risk assessments and participate in internal audits, monitoring and due diligence activities and, as appropriate, coordinate execution of follow-up actions.
• Maintain working knowledge of local industry codes and regulations as well as government enforcement actions to identify and mitigate potential compliance risks.

• Lead development of the quarterly live and transactional monitoring plan for the Europe Region in partnership with the VP, Europe Region Compliance & Ethics and the Executive Director of Global Monitoring & Remediation in the Risk Operations and Intelligence Center of Excellence.
• Conduct live and transactional monitoring of external engagement activities across the Region and generate live insight reports for incorporation into the Compliance & Ethics Central Nervous System and action by the applicable affiliate compliance lead.
• Partner with the C&E ROI COE to compile the annual monitoring insights, response and impact report for the Europe Region.
• Partner with the Executive Director, Global Risk Assessments and Insights in the C&E ROI COE to develop and implement the risk assessment protocol for the Europe Region.
• Represent BMS (speaker) at Europe Region summits and conferences focused on anti-corruption monitoring and risk assessment.

Qualifications & Experience

• 8 plus years’ experience in a pharmaceutical compliance role, with demonstrable experience leading field-based monitoring activities/teams and conducting compliance risk assessments.
• Thorough working knowledge of the ABPI and IPHA codes required.
• Expert ability to influence senior leaders (General Managers and Executive Level) and partner cross-functionally to provide practical and solution-oriented compliance guidance.
• Expert communication and interpersonal relationship skills with a demonstrated ability to support multiple elements of a comprehensive compliance program.
• Effective strategic-thinking skills with an ability to identify and recommend process improvements and best practices.
• Ability to prioritise and manage multiple projects under deadline pressure with flexibility to work on a broad range of matters.
• Language requirements: English fluency is required. Fluency in one or more Central or Eastern European languages (Polish, Czech, Hungarian or Romanian) is required. Polish language fluency strongly preferred.

Additional Requirements

• Travel requirements: Significant travel across the Europe Region (approximately 40% of the time).

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 a supportive culture, promoting global participation 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 an 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.

Bristol Myers Squibb is Disability Confident – Employer A UK Government scheme.