Director, Project Management (Late Development, Neuroscience)
Company: Disability Solutions
Location: Cambridge
Posted on: November 1, 2024
Job Description:
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:
.Position SummaryThe KarXT R&D team is looking for a Director
Project Manager (PM) to lead indication focused Sub-GPTs of the
KarXT Global Product Team (GPT).In this role, the candidate is a
key strategic partner to the KarXT Global Program Leader (GPL),
associated leadership, and cross-functional subject matter experts.
In addition to direct project management responsibilities of
assigned projects, the Director, PM will work closely with leaders
from R&D and Commercial to ensure integrated program plans are
aligned across portfolio and disease area strategy ambitions.The
Director PM is accountable for the cross-functional planning and
execution of one or more teams including definition of the
operational strategy, management of timelines, budget, risk
assessment and mitigation. The Director PM works to ensure that
cross-functional teams operate effectively, fostering positive team
dynamics and championing BMS's operating model.
Duties/Responsibilities
- General expectations of a Drug Development Project Manager (PM)
at BMS:
- The PM partners closely with the Global Program Lead (GPL) and
the Senior Project Manager (GPM) to lead sub-GPTs of the Global
Program Team (GPT) and drive the development of integrated,
efficient, and cross-functional program execution plans.
- The PM is accountable for integrated cross-functional planning
bringing together diverse functional plans and strategies,
definition of the program operational strategy, management of
timelines, budget, quality, and risk assessment and
mitigation.
- The PM will collaborate with cross-functional stakeholders to
advance BMS's portfolio of development programs in the most
efficient and effective way. The PM provides an independent voice
to shape the overall project strategy and drive optimal decisions
for the broader portfolio value.
- Director, PM (Late Development)
- At the director level, the Project Manager (PM) is accountable
for one or more Sub-GPTs of the GPT of moderate to high complexity
in the late development space and is highly autonomous in their
day-to-day work. In addition, the PM may provide oversight or
mentoring to other PMs.
- Accountable for creating and maintaining a cross-function
integrated development plan, timeline and budget for each program
and ensuring progress vs. plan.
- Facilitates effective, science-based business decisions
including the generation of multiple development scenarios/options
as needed, highlighting interdependencies and downstream impacts
(including but not limited to timelines and budget) of strategic
decisions.
- Proactively identifies risks and ensures mitigation plans are
implemented.
- Accountable for communication to team and stakeholders in a
transparent and timely manner.
- With the GPL, works to foster a high performing team and
monitor the health and operating efficiency of the team as a unit.
Leads creation of team norms and operating principles with a focus
on cross-functional input and accountability
- Develops and coordinates resource and budget planning across
functions to assure adequate resources are applied to the project
and any changes are highlighted appropriately.
- Advises on governance expectations and prepares for key
decision point discussions with focus on cross-functional input and
rigorous debate.
- For projects that are being jointly developed, works closely
with a key strategic alliance partner.
- Coaches project team members and PM colleagues to drive
excellence and accountability and develop talent pipeline for team
membership.
- Change Agent for continuous improvement and transformational
initiatives within PM function.
- Executive level presentation skills and polished written and
oral communication ability.
- Proven leader with an ability to manage multiple complex
cross-functional teams and processes in a fast-paced
environment.
- Strong analytical and decision-making ability, including
ability to synthesize complex and diverse inputs to a problem, and
recommend solutions/preferred options.
- A high level of problem-solving capability and ability to
balance competing priorities and quickly and objectively drive the
team towards a path which maximizes value.
- Must be well organized and have strong attention to detail with
an ability to deal with competing priorities; high level of
problem-solving capability and business acumen, ability to balance
competing priorities and quickly and objectively drive the team
towards a path which maximizes value.
- Strong influencing and interpersonal skills to operate and
motivate a team in a matrix environment at all levels in the
organization without authority.
- Demonstrated experience using standard program management tools
and software including integrated development plans, timelines,
risk management, and budget development and monitoring.Reporting
Relationship
- Reports into Senior Director, Project Management (also known as
the PM Group Lead)Qualifications
- Advanced degree (Ph.D. desirable) in Life Sciences, Chemical
Sciences, Physical Sciences, or other relevant discipline. In
addition, PMP certification is preferred. BS/MS degrees in a
scientific discipline in combination with 15+ years of drug
development experience will be considered.
- Late Development experience is required.
- The ideal candidate will have significant experience in
biotech/pharmaceutical/health care industry, including at least 3-5
years in project/portfolio management or leadership of
cross-functional matrix teams managing late development R&D
GPTs and associated sub-teams.
- They will need to have experience with operational study
start-up into Registrational/Phase 3 trials with a deep
understanding of the necessary steps required for NDA/BLA
submissions in the US, EU and Japan.
- Demonstrated competency in late phase drug development with
solid understanding of disease area and drug development pathway
with the ability to facilitate and 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 GPL to delve deeper to resolve issues
and challenges.
- Experience with commonly used project management tools
including but not limited to Microsoft project.
- Strong communicator able to integrate and succinctly summarize
the various parts of a project and effectively tailor messages to
audience incl. senior leaders.
- Guides teams and manages preparation of high-quality documents
and presentations for review at governance committees.
- Ensures appropriate team membership during the progression of
the program.
- 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, and cost.The starting compensation for
this job is a range from $182,000-257,000 plus incentive cash and
stock opportunities (based on eligibility).The starting pay rate
takes into account characteristics of the job, such as required
skills and where the job is performed. Final, individual
compensation will be decided based on demonstrated
experience.Eligibility for specific benefits listed on our careers
site may vary based on the job and location. For more on benefits,
please visit our BMS Career Site.Benefit offerings are subject to
the terms and conditions of the applicable plans then in effect and
may include the following: Medical, pharmacy, dental and vision
care. Wellbeing support such as the BMS Living Life Better program
and employee assistance programs (EAP). Financial well-being
resources and a 401(K). Financial protection benefits such as
short- and long-term disability, life insurance, supplementalhealth
insurance, business travel protection and survivor support.
Work-life programs include paid national holidays and optional
holidays, Global Shutdown days between Christmas and New Year's
holiday, up to 120 hours of paid vacation, up to two (2) paid days
to volunteer, sick time off, and summer hours flexibility.
Parental, caregiver, bereavement, and military leave. Family care
services such as adoption and surrogacy reimbursement,
fertility/infertility benefits, support for traveling mothers, and
child, elder and pet care resources. Other perks like tuition
reimbursement and a recognition program.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
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 . Visit 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.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: Any data processed in connection with role
applications will be treated in accordance with applicable data
privacy policies and regulations.
Keywords: Disability Solutions, Pawtucket , Director, Project Management (Late Development, Neuroscience), Executive , Cambridge, Rhode Island
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