Vice President, Global Program Lead Neuroscience

Bristol Myers Squibb

1mo ago

Job
Full-time
Expert Level
Research & Development
Healthcare
San Diego

AI generated summary

You need a relevant degree, 10+ years in drug development, leadership experience, knowledge of regulations, and a track record in clinical trial execution and cross-functional collaboration.
You will develop product strategy, manage late-stage programs, engage with health authorities, integrate commercialization inputs, lead cross-functional teams, and ensure regulatory success.

Requirements

BS/BA required, and an advanced degree preferred (MD, PhD, MBA, PharmD, etc.) must have experience in the drug development process
Proven demonstrated leadership capability; previous experience in building and leading a high performing team
A minimum of 10 years in the drug development & commercialization process, Health Authorities and/or academic experience, and clinical trial design with proven progression in relevant roles
Significant experience in related therapeutic area
Extensive working knowledge in the end-to-end drug development process, along with expertise in one or more of the relevant areas (e.g., clinical, regulatory, project planning and management, medical, commercial development)
Prior experience in building a development plan that was aligned with a broader strategy (TA/Franchise) and endorsed by governance
Experience in building trusting cross-functional stakeholder partnerships in a matrix organization
Demonstrated ability to constructively influence peers and senior leaders across the enterprise
Working knowledge of regulations in the pharmaceutical industry (US and Global preferred)
Demonstrated ability to effectively collaborate across geographic and functional boundaries (e.g. early development, R&D, disease strategy teams, marketing, access, etc.) and building strong external relationships
Ability to navigate through a complex and dynamic healthcare environment
Track record of successfully executing on large, complex projects, with a preference for successful drug trial oversight and execution
Abreast of scientific issues as they impact business development and strategic planning
Success in situations requiring rigorous, analytical problem solving and the ability to determine scientific opportunity and commercial targets
Broad understanding of domestic and international issues relative to the pharmaceutical industry
Proven agility in prioritizing and navigating competing demands
For late development projects, prior submission experience is highly preferred

Responsibilities

Develops and manages product strategy and late drug development program to ensure approval and commercial success
Defines and executes the strategic integrated development plan (IDP) in partnership with the cross functional GPT members
Participates in regulatory filings (NDA, BLA filings) as well as develops strategy for orphan drug designation
Engages with Health Authorities and/or Advisory Committees
Leads team to develop program strategy and clinical program, commercialization strategy plans, business case development, and understands how access, pricing and reimbursement needs for supporting value proposition will inform trial design
Builds and maintains collaborative relationships with external stakeholders (Opinion Leaders, Strategic Alliance Partners, Patient Advocacy Leaders, Health Authorities) and appropriately incorporates insights and advice to maximize program impact
Actively supports Investor Relations and Public Affairs in managing external BMS communications
Integrates commercialization inputs and deliverables to design the late program strategy that enables approval of a meaningfully differentiated asset with potential to maximize asset value
Understands necessary commercial inputs needed to inform the end-to-end development process leading to regulatory approval and successful commercialization
Integrates market inputs (e.g., TPP, DEX/VAP, CI insights) into the integrated development plan, incl., clinical plans and labeling strategy; Appreciates translation of clinical data into claims and considerations for label development
Understands and contributes to development of forecasts and investment scenarios, how to assess risk and conduct valuations, and implications for decision making
Contributes to the development of brand hallmarks and brand strategy (generic name, brand name, logo, brand colors, positioning, messaging, campaign, segmentation, promotional strategy) understanding the relationship to clinical trial design
In partnership with Medical Affairs, supports development of KOL plans and engagements, and leverages KOL input in context of development programs and communicating evidence
Supports commercial needs and recommendations to guide CMC and GPS on trade packaging and commercial product
Utilizes various resources to design clinical trials that are competitively differentiating (e.g., competitive intelligence knowledge, KOL input)
Actively participates with Health Authorities in finalizing clinical design and adequate endpoints
Understands clinical trial operational complexities from study start up through enrollment, quality assurance, and study readout
Has an active role in analysis and/or interpretation of clinical data and translation into scientific communication strategy, including publications, and commercial strategy
Understands and reflects the impact of VAP inputs (Early Access Review and DEX recommendations, commercial opportunity assessment, TOP/TPP requirements, and value drivers as inputs in clinical trial design
Inclusively Collaborates Across the BMS Matrix with an Enterprise Mindset Effectively collaborates with matrix functions by building trust and driving toward the collective success of the program
Demonstrates Enterprise Mindset Problem-Solving and Decision Making Gathers diverse perspectives assess alternate resolutions and makes thoughtful, informed Enterprise decisions
Develops and Leads a High Performing Matrix Team Builds, leads and inspires high performing cross functional matrix team through a unified program strategy on behalf of our patients
Holds Oneself and Others Accountable Takes initiative to address challenges, removes barriers, holds others accountable for the collective success of the program outcomes and team collaboration
Demonstrates Character Leads with the values, self-awareness, and humility, seeks feedback, Includes integrity

FAQs

What is the role of the Vice President, Global Program Lead Neuroscience at Bristol Myers Squibb?

The Vice President, Global Program Lead Neuroscience is accountable for leading the Global Program Team and orchestrating the design and execution of a global integrated program strategy from candidate nomination through drug development to successful launch and commercialization.

What qualifications are required for this position?

A BS/BA is required, with an advanced degree preferred (MD, PhD, MBA, PharmD, etc.), along with at least 10 years of experience in the drug development and commercialization process, including leadership capability and experience in related therapeutic areas.

Is industry experience necessary for this role?

Yes, significant experience in drug development and commercialization, particularly in the relevant therapeutic area, is required.

What kind of responsibilities will I have in this position?

Responsibilities include developing product strategy, engaging with Health Authorities, integrating commercialization inputs, designing clinical programs, and leading a high-performing cross-functional matrix team.

Are there opportunities for career growth and opportunities at Bristol Myers Squibb?

Yes, Bristol Myers Squibb offers unique opportunities for professional growth and the chance to work on transformative projects that can change the lives of patients.

What is the compensation range for this position?

The starting compensation range for this role is between $341,360 and $413,648, with additional incentive cash and stock opportunities based on eligibility.

Does Bristol Myers Squibb offer benefits for employees?

Yes, Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs, including medical, pharmacy, dental, vision care, financial well-being resources, and various work-life programs.

How does Bristol Myers Squibb support work-life balance?

The company recognizes the importance of balance and flexibility in the work environment and provides various programs that allow employees to pursue their goals both at work and in personal life.

What type of work environment does Bristol Myers Squibb promote?

Bristol Myers Squibb promotes a supportive culture that values passion, innovation, accountability, inclusion, and integrity, encouraging global participation in clinical trials and collaboration among teams.

Is prior experience with regulatory bodily submissions preferred for this position?

Yes, prior submission experience, especially for late development projects, is highly preferred.

Bristol Myers Squibb

Manufacturing & Electronics

Industry

10,001+

Employees

Mission & Purpose

At Bristol Myers Squibb, we work every day to transform patients’ lives through science. That work inspires some of the most interesting, meaningful, and life-changing careers you’ll experience. Join us and pursue innovative ideas alongside some of the brightest minds in biopharma, collaborating with a team rich in diversity of experiences, and perspectives. We have built a sustainable pipeline of potential therapies and are leveraging translational medicine and data analytics to understand how we can deliver the right medicine to the right patient, at the right time, to achieve the best outcome. Whether in a scientific, business or supporting function, a career at BMS means you’ll be inspired every day to grow and thrive through opportunities that are uncommon in scale and scope. Here, you’ll be on the cutting edge of powerful innovation in oncology, hematology, immunology, cardiovascular disease, and fibrosis, with colleagues united in the mission to help patients. Through the Bristol Myers Squibb Foundation, we also promote health equity and seek to improve health outcomes of populations disproportionately affected by serious diseases and conditions. Our mission is to give new hope to help patients prevail over serious disease – it drives everything we do.