Vice President, Global Program Lead
vor 2 Wochen
**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.
**Vice President, Global Program Lead - Cell Therapy**:
The Global Program Lead for the GPRC5D program in Multiple Myeloma is an enterprise leader overseeing and leading the cross-functional matrix team with accountability for all critical deliverables from manufacturing to clinical development and commercialization.
**Technical/Functional 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
**Clinical Trial Design, Execution, and Interpretation**
- 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
**Leadership **Responsibilities**:
- **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
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