Manager, Clinical Project Management, Oncology

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

Job Function:
R&D Operations

Job Sub Function:
Clinical Trial Project Management

Job Category:
Professional

All Job Posting Locations:
Beerse, Antwerp, Belgium, Leiden, Netherlands

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for Manager, Clinical Project Management, Oncology in Beerse, Belgium and Leiden, Netherlands.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.

While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

Belgium - Requisition Number: R-010432

Netherlands - Requisition Number: R-010432

United Kingdom - Requisition Number: R-010432

United States- Requisition Number: R-009099

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Purpose: The Manager, Clinical Project Management (CPM) 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. 

You will be responsible for:


* 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 resour...