Manager, Clinical Project Manager, Immunology

Johnson & Johnson is recruiting for a Manager, Clinical Project Manager. The position can be located in the US (Titusville, NJ; Spring House, PA; Raritan, NJ; Horsham, PA; La Jolla, CA) or EMEA (Beerse, Belgium; Basel, Switzerland; High Wycombe, United Kingdom; Cork, Ireland; Leiden, Netherlands).

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/ .

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential. At Johnson & Johnson, we all belong.

The Manager, Clinical Trial Leader Project Management (CTPM) is responsible for the creation and management of the integrated project schedule.

They will collect, consolidate and report budget, timeline and FTE actuals vs. plan and will identify potential issues for the trial through active management of the study schedule.

They enable decision making by developing scenarios that reveal potential cost, timeline, and budget impacts. They play a key role in maintaining visibility to and documentation of current plans, scenarios under consideration, and changes in direction for study level plans. They are also responsible for ensuring planning systems align with the compound development plan and the integrated project schedule.

Principal Responsibilities:

• Create, manage, and maintain integrated study schedule in MS Project, including KEMs, Roadmaps, and critical path visualization aligning in PLW.

• Clinical timelines in PLW align to MSP schedule and coordinate the integrated clinical plan with CDT project plans. Ensure proper resource demand is reflected.

• Develop scenarios in PLW for budget, timeline, and FTE forecasting, while generating situational operational scenarios.

• Collect, consolidate, and report financial, timeline and resource data for governance approvals and external funding partnerships. Manage scope control, FTE and OOP variances.

• Document key decisions, actions, risks, issues, and lessons learned, as well as maintain applicable trial governance documentation.

• Provide support for Clinical PM reporting (i.e., the PLW team list).

Additional Responsibilities may Include:

Foster employee engagement, inclusion, and Credo Behaviors.

Principal Relationships:

Internal: Clinical Trial Leaders, Clinical Trial Managers, Clinical Trial Assistants, DAS Leaders, Trial Management Directors, representatives of Delivery Operations, representatives of other GD and non-GD Functions and Clinical Teams