Specialist, Project Planning
Company: Disability Solutions
Location: Princeton
Posted on: May 7, 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:
careers.bms.com/working-with-us .Position SummaryAs a partner with
stakeholders across all stages of drug development, the Project
Planner ensures appropriate modeling of development plans within
enterprise systems to enable planning and decision making by
development teams, functional areas, and governance.Key
Responsibilities
- Coordination and creation of country timelines and metrics for
clinical studies in partnership with Resource Management and
Regional Clinical Operations.
- Perform ongoing review and management of country details and
timeline analysis to highlight inconsistencies, scheduling
conflicts, and gaps in country models compared to scheduling
standards. Ensure data quality of current plans.
- Coordination and creation of projects, studies, timelines and
metrics for Medical studies in partnership with Medical Project
Management and Global Development Operations.
- Perform ongoing review and management of Medical study details
and timeline analysis to highlight inconsistencies, scheduling
conflicts, and gaps in country models compared to scheduling
standards. Ensure data quality of current plans.
- Coordination and creation of projects, studies, timelines and
metrics for Research Projects in partnership with TRCs and Research
leadership.
- Perform ongoing review and management of Research Project
details and timeline analysis to highlight inconsistencies,
scheduling conflicts, and gaps in Research projects compared to
scheduling standards. Ensure data quality of current plans.
- Clear and transparent communication of timelines and key
deliverables with functional team representatives, key functional
stakeholders, and Resource Managers.
- Participate in other team-based assignments such as
coordination of project-based budgeting required for annual budget
process and department capability/capacity
initiatives.Qualifications & Experience
- A Bachelor's degree in science or engineering with 1+ years of
experience in pharmaceutical research, development, or
commercialization with direct experience related to scheduling
creation, planning, and management is required.
- An advanced degree (e.g., MS, MBA) is a plus.
- This position requires experience in the pharmaceutical
industry with a fundamental understanding of drug development and
commercialization practices.
- Experience with scheduling methodologies as well as
technological literacy with computer applications necessary to
create, manage and analyze project schedules and timelines is a
must.
- Experience with Planisware, Clinical Trial Management Systems,
and reporting tools is a plus.#LI-HybridIf 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 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.
Keywords: Disability Solutions, Trenton , Specialist, Project Planning, Other , Princeton, New Jersey
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