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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: Director HemOnc Medical Early Assets Differentiation and Pipeline (EDAP)
ROLE SUMMARY
Executive Director (ED) HemOnc Medical (EDAP) will lead a team to provide early and ongoing medical input across Hematology/Oncology Early Portfolios to drive clinical differentiation and maximize health outcomes early clinical adoption and patient access across Hematology and Oncology Therapy areas. The goal of this function is to expand the clinical value and patient reach of the early portfolio assets.
This is a senior medical leadership role reporting to the VP Medical Early Assets Innovation & Differentiation Strategy of and will be a member of their Leadership Team.
Location: New Jersey
Responsibilities:
Accountable for leading a team of senior medical affairs professionals focusing on BMS early pipeline that ensures optimal differentiation access and proof of concepts for our early pipeline expanding the value of the early pipeline
Responsible for shaping the early portfolio narrative and communicating its strategy internally and externally. Leverage knowledge of the medical landscape including a strong understanding of medical affairs strategies and tactics for early phase clinical assets.
Inform and accelerate governance decisions on priority programs to ensure maximum transformational clinical value is captured via CDP and IEP.
Make recommendation to research and clinical development teams on based external landscape and insights from scientific partnerships and external experts.
Implement an integrated approach to differentiating drug therapies including enhancing the future value proposition to patients HCPs and payers worldwide.
Build early scientific partnerships councils and research collaborations at top centers of excellence for research and with patients when applicable
Leverage an understanding of anticipated changes in Policy/Payor/Clinic models in US and EU Japan Asia and LatAm to guide development strategies.
Represent medical perspective in business development.
Understand the role of correlative assays and diagnostic platforms in determining treatments across diseases of interest and integrate this understanding into early program strategic approaches.
Ensure that execution of a comprehensive medical communications plan (including publication planning) is integrated into priority asset plans.
Identify and execute opportunities for medical affairs enabled signal generation for priority assets leveraging internal organization as well as external trusted centers of excellence.
Leverage novel approaches to integrating patient journey insights into early compound differentiation strategies.
In this role you will:
Focus on early pipeline namely assets in Phase 1 and Phase 2 signal seeking development.
Maintain an ongoing dynamic prioritization of assets in partnership with discovery and early development teams to ensure efforts are invested in the most promising asset.
Lead a team of senior medical affairs professionals to ensure the development and execution of strategies that drive clinical differentiation and ensure successful fit to clinic.
Work across the Oncology Therapeutic Area (TA) (Hematology and Oncology) with tailored approaches to each market.
Bring a patient lens and perspective to early development and ensure plans are reviewed with external stakeholders.
Provide leadership in relation to biomarkers and CDx as well as potential clinical applicability/utility.
Leverage an understanding of anticipated changes in Policy/Payor/Clinic models in US and EU Japan Asia and LatAm to guide strategies.
Enhance the differentiated clinical value and leadership of our early portfolio by shaping the design and implementation of innovative biomarker diagnostic test diagnostic platform software and big data solutions and strategic collaborations.
Partner with the Oncology TA teams to align early pipeline strategies with TA strategies.
Partner with a crossfunctional team to create to create a clear and compelling scientific story for portfolio and individual compounds.
Oversee early pipeline strategy for medical congresses and pipeline scientific communication are tied to strategy for all congresses
Partner in building internal and external communication strategies/tactics.
Build and leverage a broad network of external expert relationships to inform insights and innovation.
Identify potential collaborations (COEs) and drive nonTA specific scientific partnerships for early development.
Perform diligence for to support BD&L efforts.
Delivery on this mandate requires highlevel stakeholder engagement and collaboration skills delivered through indirect leadership/influencing behaviors within Medical and Cross Functional leadership.
Required qualifications and experiences:
MD PhD or PharmD
10 years of diverse experience in development clinical medical and commercial roles focusing on Global or marketbased Medical Affairs.
Previous commercial launch experience preferably at local country level.
Previous disease specific experience (35 years).
Prior experience in either Medical or Development preferred
Previous commercial experience is preferred
Business development experience preferred
#LIHybrid
If you come across a role that intrigues you but doesnt 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 Lifechanging 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.
Onsite Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes siteessential sitebydesign fieldbased and remotebydesign jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Siteessential roles require 100% of shifts onsite at your assigned facility. Sitebydesign 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 fieldbased and remotebydesign 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 . Visit to access our complete Equal Employment Opportunity statement.
BMS cares about your wellbeing and the wellbeing of our staff customers patients and communities. As a result the Company strongly recommends that all employees be fully vaccinated for Covid19 and keep up to date with Covid19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position please visit this page for important additional information: data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Required Experience:
Director
Full-Time