Associate Director Project Management - Cell Therapy

Profile

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

PURPOSE AND SCOPE OF POSITION:

Associate Director Project Management is responsible for the direction, coordination, implementation, control and completion of projects, while remaining aligned with company strategy, commitments and goals. Assoc Dir PM oversees initiating, planning and executing Cell Therapy Development and Operations (CTDO) programs and projects. The primary focus of the CTDO PM will be to manage critical projects in support of specific product programs and/or building CTDO infrastructure. This includes partnering with the project leads to identify scope, work and project strategy. The PM is responsible for developing detailed project plans in support of the project scope and cross-functional stakeholders. This position works closely with the drug product and vector CMC Project Leads and PMs in order to coordinate and organize the deliverables associated with the CTDO product programs. This position will also work closely with functional leadership and representatives to ensure alignment and coordination across CTDO priorities.

The Associate Director-Level PM will be responsible for using and promoting CTDO PMO best practices, tools and templates. CTDO PMs may be called upon to provide training and coaching for functional project managers. The successful candidate will support development of a robust CTDO PMO: share ideas, tools, best practices, training, lessons learned, establish core competencies, conduct peer reviews of project management deliverables, etc. Key business processes include, but not limited to, leading strategic project planning and goal setting, project prioritization and portfolio alignment, project execution, project documentation and archival, and process improvement, standards development, resource modeling and metrics.

The successful candidate will be a demonstrated leader with the breadth of professional experience and the drive to work with both internal and external partners to define and implement effective project management plans. Must have the ability to work in a highly matrixed and cross-functional organization, against tight deadlines, and with world-class partners, suppliers and business leaders alike.

REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:

Education:


Bachelor’s degree in Life Sciences-related discipline

Advanced degree in Life Sciences-related discipline and/or an MBA strongly preferred

Project management qualification; PMI’s Project Management Professional (PMP) or equivalent


Experience


10 years’ experience in bio tech/life sciences project management

Experience in cellular therapy is preferred





PMP certification required; PMO experience preferred

Proficiency with related software tools such as: MS Project, OnePager, SmartSheets, MS PPT, MS Excel, etc.

Experience in Agile teams

Strong knowledge of biopharma industry

Excellent interpersonal, communication, and presentation skills

Ability to work cross-functionally, with matrixed teams; maintaining strong business partner relationships

Strong leadership and communication skills

Expertise in conflict resolution

Excellent problem-solving skills

Willingness to do what needs to be done in a dynamic environment


DUTIES AND RESPONSIBILITIES:


Partner with project lead to successfully achieve project objectives

Provide strong team leadership and drive to ensure projects are executed on-time and within budget

Facilitate the definition of project scope, goals and deliverables

Create project plans; scope, work, resources, scheduling, etc.

Maintain project objectives through project life cycle

Monitor execution and quality to customer/stakeholder/sponsor standards

Identify and resolve issues and risks

Report on project progress, offer viable solutions and opportunities as they arise

Implement appropriate project change control

Manage resources to make sure schedule is on track

Facilitate all project team meetings; attend related project team meetings as necessary to ensure alignment

Evaluate and assess result of project

Provide structure and leadership across departments to ensure team meets project objectives

Work with internal and external stakeholders to manage project deliverables, e.g. CMO’s, Supply Chain, etc.

Develop and communicate status to PMO, Project and CTDO Leadership


WORKING CONDITIONS (US Only):

Work is primarily conducted in an office environment with a mix of natural and LED lighting with low level background noise. Required computer and conferencing hardware are provided. 80% time seated desk work with ergonomic working spaces and sit/stand desks

Local, national and international travel may be required up to 25%.

This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

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 the resources to pursue their goals, both at work and in their personal lives.

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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