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

The Associate Director, Portfolio Management Insights, Portfolio & Strategic Operations (P&SO), drives portfolio management insights development and delivery to the Global Program Teams (GPTs), Therapeutics Areas (TAs) leaders, Hematology Oncology Cell Therapy (HOCT)/Immunology Cardiovascular Neuroscience (ICN) leadership, crucial for strategic decision-making within the drug development portfolio. Established in October 2023, this is a new capability at BMS with the vision to become a Drug Development Operational Portfolio Management Insights center, working across the enterprise, including P&SO leads, Business Insights & Analytics (BI&A), Commercial Portfolio Strategy, P&SO Resource management & planning, R&D Finance, and other enterprise functions.

This role reports to the Executive Director, Drug Development Portfolio Strategy Implementation & Reporting (PSI&R), part of the Portfolio & Resource Management (P&RM) team. The ideal candidate will possess an understanding of drug development, coupled with advanced data acumen and experience in analyzing and delivering operational portfolio insights to enable data-driven decisions and effective risk management, ultimately enhancing productivity across drug development.

Key Responsibilities

Provides ‘fit-for-purpose’ portfolio insights to GPT, HOCT & ICN leadership, and TA leadership to enable proactive risk management and cross-functional resource optimization​, build awareness and visibility into corporate pipeline goals, priority pipeline execution, and portfolio spend & resource management, in collaboration with P&SO Leads.

• Drives development of insights to amplify visibility into critical risks at the GPT, TA, and portfolio levels, informing discussions & decisions by key stakeholders - GPTs, TAs, HOCT/ ICN leadership

• Supports evolution of and delivers insights for the portfolio spend and resource calibration analyses across Drug Development organization, in close partnership with R&D Finance and P&SO Resource management & planning.

Partners with Commercial Portfolio Strategy & BI&A to bring integrated analytics to key DD stakeholders, enabling real-time portfolio prioritization at the governance forums informed by operational insights, risk management at the key inflection points in drug development pipeline.

Develops and delivers clear and concise presentations of portfolio insights.​

Supports DD portfolio management: proactively identifies, and escalates operational execution risks that require TA, ICN/HOCT leadership, and Drug Development leadership team (DDLT) action​s.

Supports continuous evolution of pipeline reporting to DDLT and BMS leadership

Qualifications & Experience

6+ years of professional experience in the life sciences or biopharmaceutical industry

Expertise in biopharmaceutical Data Science and Statistical analysis preferred.

Degree in Life Sciences or Business Management, and/or advanced degree in related discipline preferred (e.g., PhD, MS, MBA)​.

Business operations experience and familiarity with divisional management​.. Expertise in R&D functions (e.g., Clinical Operations, CMC, Regulatory, Project management, Commercial) preferred.

Demonstrated understanding of drug development, portfolio prioritization, strategy, and execution.​

Demonstrated strength in partnering across R&D and with business leaders to assess critical needs and operational pipeline performance.​

Comfort in an agile work environment and capable of bringing structure to vaguely defined problems while using creative yet pragmatic problem-solving approaches.​

Strong communication and interpersonal skills, with the ability to interface with a broad range of internal and external stakeholders at all levels of the organization.​

Proactive, organized, and promoter of diversity and inclusivity​

Highly effective verbal and written communication skills; strong change & stakeholder management skills.​

Ability to build relationships and influence, and drive organizational engagement across functions and sites.

#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: R1581699

Updated: 2024-06-03 03:15:54.776 UTC

Location: Lawrence Township-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.