Director, Drug Development Project Manager - Early Assets (Oncology, Hematology, and Cell Therapy) - Bristol-Myers Squibb
Princeton, NJ 08543
About the Job
Working with UsChallenging
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.Early Development Project Managers (ED PMs) provide execution leadership for an asset or a portfolio of assets for a Therapeutic Area (TA)/Thematic Research Center (TRC)
They partner with the Early Development Program Leads (EDPLs) to lead cross-matrix Early Development Program Teams (EDPTs) that are the hub of drug development activities at BMS, shaping and executing the drug development strategies from Candidate Declaration through Phase 2 Proof of Concept
The ED PMs sit in the Research & Early Development Project Management (R&ED PM) organization within R&D Strategy and Planning (RDSP)
This role supports the portfolio of Non-oncology, including immunology, cardiovascular, fibrosis and neuroscience assets. This position can sit in Cambridge; Princeton or Summit, NJ; Seattle; San Diego or Brisbane, CA; and allows for a hybrid work arrangement
**level is commensurate with experience and determined during the interview process**The Director, Early Development Project Manager (ED PM) is a seasoned project manager who is accountable for the cross-functional planning and execution of one or more drug development programs, including a definition of the operational strategy, management of timelines, cost, quality, and risk assessment and mitigation
The ED PM provides an independent voice to shape the overall project strategy and drive optimal decisions for the broader portfolio value
They also are champions of the project management role and support, championing and execute on the R&ED PM and RDSP vision to enable an industry-leading PM organization.Roles & Responsibilities: The Early Development Project Manager (ED PM) is accountable for one or more EDPTs of moderate or high complexity and is highly autonomous in supporting the Hematology/Oncology/Cell Therapy portfolio as part of their day-to-day work. Partners with the Early Development Program Lead (EDPL) to lead a cross-functional matrix team of experts in advancing programs/assets within their Early Development Program Team (EDPT) remit
Acts as an integrator within the EDPT and across the enterprise to ensure alignment on project strategy implementation in alignment with project priority, across all intended indications and for all geographies.Accountable for creating and maintaining a cross-functional development plan, timeline, and budget for each program and ensuring progress vs
plan.Facilitates effective, science-based business decisions, including the development of scenarios (base-case, buy-ups, buy-downs) as needed, highlighting interdependencies and downstream impacts (including but not limited to timelines and budget) of strategic decisions.Proactively identifies and facilitates team review of program risks and ensures mitigation plans are developed and implemented.Ensures all decisions are assessed as to their risks and impacts
Accountable for communication with team and stakeholders in a transparent and timely manner.The EDPL fosters a high-performing team and monitors the health and operating efficiency of the group as a unit
Leads creation of team norms and operating principles with a focus on cross-functional input and accountability and robust analysis of vetted options and decision-making per guidance framework.Coaches project team members and others to drive excellence and accountability and develop a talent pipeline for DPT membership.Ensures appropriate DPT membership during the progression of the program. Develops and coordinates resource and budget planning across functions to ensure adequate resources are applied to the project, and any changes are highlighted appropriately.Advises on governance expectations and prepares for critical decision-point discussions with a focus on cross-functional input, and rigorous debate to enable efficient decision-making.For projects that are being jointly developed, works closely with a key strategic alliance partner.As a project management subject matter expert, understands best practices, identifies gaps and challenges, implements efficiencies, and improves ways of working within R&ED PM and RDSP.Acts as a change agent for continuous improvement and transformational initiatives developed within R&ED PM and RDSP.Requirements:Advanced degree in Life Sciences, Chemical Sciences, Physical sciences, or other relevant disciplines., MS/Ph.D
preferred.Minimum of 10-15 years of experience in the biotech/pharmaceutical industry, preferably in the early development space, including seven years in project/portfolio management or leadership of cross-functional matrix teams.Demonstrated competency in early phase drug development expertise with a solid understanding of disease area and drug development pathway with the ability to contribute to strategic discussions. Leadership skills including situational leadership, ability to lead a team of experts and influence without authority.Demonstrated ability to lead matrix teams, knows how to work at the strategic level with the DPL and when to delve deeper to resolve issues and challenges.Experience with commonly used project management tools, including but not limited to Microsoft projects.A strong communicator can integrate and briefly summarize the various parts of a project and effectively tailor messages to the audience, incl
senior leaders.Ability to resolve complex problems and manage difficult stakeholder situations.Ability to lead the development of critical path analyses and scenario planning.Excellent Project Management Skills – drives execution while balancing speed, quality, risk, and cost.The starting compensation for this job is a range from $173,000-217,000, plus incentive cash and stock opportunities (based on eligibility). The starting pay takes into account characteristics of the job, such as required skills and where the job is performed.Final, individual compensation is decided based on demonstrated experience.For more on benefits, please visit our BMS Careers site.Eligibility for specific benefits listed in our careers site may vary based on the job and location.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 CareersWith 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.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 careers.bms.com/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.
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.Early Development Project Managers (ED PMs) provide execution leadership for an asset or a portfolio of assets for a Therapeutic Area (TA)/Thematic Research Center (TRC)
They partner with the Early Development Program Leads (EDPLs) to lead cross-matrix Early Development Program Teams (EDPTs) that are the hub of drug development activities at BMS, shaping and executing the drug development strategies from Candidate Declaration through Phase 2 Proof of Concept
The ED PMs sit in the Research & Early Development Project Management (R&ED PM) organization within R&D Strategy and Planning (RDSP)
This role supports the portfolio of Non-oncology, including immunology, cardiovascular, fibrosis and neuroscience assets. This position can sit in Cambridge; Princeton or Summit, NJ; Seattle; San Diego or Brisbane, CA; and allows for a hybrid work arrangement
**level is commensurate with experience and determined during the interview process**The Director, Early Development Project Manager (ED PM) is a seasoned project manager who is accountable for the cross-functional planning and execution of one or more drug development programs, including a definition of the operational strategy, management of timelines, cost, quality, and risk assessment and mitigation
The ED PM provides an independent voice to shape the overall project strategy and drive optimal decisions for the broader portfolio value
They also are champions of the project management role and support, championing and execute on the R&ED PM and RDSP vision to enable an industry-leading PM organization.Roles & Responsibilities: The Early Development Project Manager (ED PM) is accountable for one or more EDPTs of moderate or high complexity and is highly autonomous in supporting the Hematology/Oncology/Cell Therapy portfolio as part of their day-to-day work. Partners with the Early Development Program Lead (EDPL) to lead a cross-functional matrix team of experts in advancing programs/assets within their Early Development Program Team (EDPT) remit
Acts as an integrator within the EDPT and across the enterprise to ensure alignment on project strategy implementation in alignment with project priority, across all intended indications and for all geographies.Accountable for creating and maintaining a cross-functional development plan, timeline, and budget for each program and ensuring progress vs
plan.Facilitates effective, science-based business decisions, including the development of scenarios (base-case, buy-ups, buy-downs) as needed, highlighting interdependencies and downstream impacts (including but not limited to timelines and budget) of strategic decisions.Proactively identifies and facilitates team review of program risks and ensures mitigation plans are developed and implemented.Ensures all decisions are assessed as to their risks and impacts
Accountable for communication with team and stakeholders in a transparent and timely manner.The EDPL fosters a high-performing team and monitors the health and operating efficiency of the group as a unit
Leads creation of team norms and operating principles with a focus on cross-functional input and accountability and robust analysis of vetted options and decision-making per guidance framework.Coaches project team members and others to drive excellence and accountability and develop a talent pipeline for DPT membership.Ensures appropriate DPT membership during the progression of the program. Develops and coordinates resource and budget planning across functions to ensure adequate resources are applied to the project, and any changes are highlighted appropriately.Advises on governance expectations and prepares for critical decision-point discussions with a focus on cross-functional input, and rigorous debate to enable efficient decision-making.For projects that are being jointly developed, works closely with a key strategic alliance partner.As a project management subject matter expert, understands best practices, identifies gaps and challenges, implements efficiencies, and improves ways of working within R&ED PM and RDSP.Acts as a change agent for continuous improvement and transformational initiatives developed within R&ED PM and RDSP.Requirements:Advanced degree in Life Sciences, Chemical Sciences, Physical sciences, or other relevant disciplines., MS/Ph.D
preferred.Minimum of 10-15 years of experience in the biotech/pharmaceutical industry, preferably in the early development space, including seven years in project/portfolio management or leadership of cross-functional matrix teams.Demonstrated competency in early phase drug development expertise with a solid understanding of disease area and drug development pathway with the ability to contribute to strategic discussions. Leadership skills including situational leadership, ability to lead a team of experts and influence without authority.Demonstrated ability to lead matrix teams, knows how to work at the strategic level with the DPL and when to delve deeper to resolve issues and challenges.Experience with commonly used project management tools, including but not limited to Microsoft projects.A strong communicator can integrate and briefly summarize the various parts of a project and effectively tailor messages to the audience, incl
senior leaders.Ability to resolve complex problems and manage difficult stakeholder situations.Ability to lead the development of critical path analyses and scenario planning.Excellent Project Management Skills – drives execution while balancing speed, quality, risk, and cost.The starting compensation for this job is a range from $173,000-217,000, plus incentive cash and stock opportunities (based on eligibility). The starting pay takes into account characteristics of the job, such as required skills and where the job is performed.Final, individual compensation is decided based on demonstrated experience.For more on benefits, please visit our BMS Careers site.Eligibility for specific benefits listed in our careers site may vary based on the job and location.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 CareersWith 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.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/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.
Source : Bristol-Myers Squibb