Clinical Project Manager – Immunology

☞ Johnson & Johnson

看过: 104

更新日: 13-11-2025

位置: Beerse Antwerp

类别: 规划/项目 IT-软件

行业: Hospitals Health Care

工作类型: Full-time

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工作内容

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

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 anExperienced Analyst, Product Portfolio Liaisonto be in Beerse, Belgium.

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):

United States - Requisition Number: R-001077

Belgium – Requisition number: R-004929

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

Purpose

The Clinical Project Manager (CPM) is responsible for comprehensive and effective project planning, execution, monitoring and close-out of all clinical trials ensuring cross- functional alignment. The CPM is an individual contributor who is a developing subject matter expert working independently with minimal supervision while also coaching others. They are expert in scenario building and CPM processes as well as tools such as MS Project, Planisware, OnePager, as well as analytics and reporting. They are proficient in planning and forecasting.

In this role the CPM serves as a proactive leader working cross functionally to close gaps between functions, deliverables, and trial teams. They will collect, consolidate, and report budget, timeline and FTE actuals vs. plan and will identify potential issues for the trial through active risk and budget management. They will empower teams to take ownership of decision making, providing guidance and support to frame discussions, encourage diverse points of view while enabling strategic alignment to project goals.

You Will Be Responsible For

  • Create, manage, and maintain integrated study schedule in MS Project, including Key Event Maps, Roadmaps, and critical path visualization aligning in Planisware.
  • Assure Clinical timelines in Planisware align to MS Project schedule and coordinate the integrated clinical plan with Clinical Development Team project plans. Ensure proper resource demand is reflected.
  • Develop scenarios in Planisware 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 Out of Pocket variances.
  • Ensure key decisions, risk, and scope changes are captured, drive after action reviews as well as maintain trial governance documentation.
  • Identify and implement opportunities for continuous improvement as needed
  • Provide support for team-based reporting (i.e., the Planisware team list).
  • Mentor & support onboarding of new team members, particularly those in Trial Management.

Education

Qualifications / Requirements:

  • Bachelor’s degree is required

Required

  • Minimum of 6-8 years in Pharmaceutical, Healthcare or related industries
  • Strong Project Management experience
  • Must possess excellent leadership skills and proven ability to foster team productivity and cohesiveness
  • Experience leading without authority and in multi-functional matrixed and global environments
  • Excellent decision-making, analytical and strong financial management skills
  • Ability to mentor and coach others
  • Ability to support and participate in the training, development, and evaluation of staff on a regular basis
  • Strong communication and presentation skills
  • Up to 10% travel – Domestic & International

Preferred

  • Knowledge of Clinical Operations, MSP, Planisware, OnePager
  • Experience managing multiple aspects of the execution of global clinical trials

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最后期限: 28-12-2025

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