Manager, Project Planning - Princeton, United States - Bristol-Myers Squibb

Mark Lane

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Mark Lane

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Description

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.


Position Summary


As a partner with global project managers 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

  • Creation and management of complex project timelines using BMS Planisware enterprise system and associated scheduling tools according to established best practices." Management of target dates and study drivers for key activities in collaboration with core team representatives." Identification and communication of timeline and scope risks and issues to Project Manager (PM).
  • Perform asset timeline and Book of Work (BOW) analysis to highlight inconsistencies, scheduling conflicts, and gaps in asset models 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, Resource Managers, and Finance Resource Managers.
  • Partner with PM to lead and manage BOW focused discussions and support submission timeline development and tracking." Additionally, assist PM with project work when appropriate.
  • Participate in other teambased assignments such as coordination of projectbased 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 Planisware, Clinical Trial Management Systems, and reporting tools is a plus.

Uniquely Interesting Work, Life-changing Careers

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 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.

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