Clinical Project Manager, Senior Analyst
Job Summary
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at .
As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
R&D OperationsJob Sub Function:
Clinical Trial Project ManagementJob Category:
ProfessionalAll Job Posting Locations:
Beerse Antwerp BelgiumJob 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.
US: Spring House PA or Raritan NJ or Titusville NJ - Requisition Number: R-070513
Beerse BE - Requisition Number: R-071013
Remember whether you apply to one or all of these requisition numbers your applications will be considered as a single submission.
We are searching for the best talent for Clinical Project Manager Senior Analyst.
The Clinical Project Manager 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 and risk log.
Primary responsibilities:
- 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.
- Document key decisions actions risks issues and lessons learned as well as maintain trial governance documentation.
- Ensure risks are captured and monitored
- Ensure budgets are effectively managed and forecasts adjusted to reflect current thinking
- Drive and facilitate after action review meetings and results are documented
- Work with the team to assess and remediate impact to scope budget timelines
- Provide support for team-based reporting
- Mentor & support onboarding of new team members particularly those in Trial Management.
Qualifications:
Education:
- Bachelors degree required
Required:
- Minimum of 4 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
- Strong communication and presentation skills
- Up to 10% travel Domestic & International
Preferred:
- Knowledge of Clinical Research Operations
- 2-3 years of experience managing multiple aspects of the execution of global clinical trials (Phases I-IV)
This job posting is anticipated to close on April 28 2026. The Company may however extend this time-period in which case the posting will remain available on to accept additional applications.
#LI-Hybrid
Required Skills:
Preferred Skills:
Analytical Reasoning Clinical Research and Regulations Clinical Trial Designs Clinical Trial Management Systems (CTMS) Clinical Trials Communication Data Savvy Laboratory Operations Organizing Problem Solving Productivity Planning Professional Ethics Project Integration Management Quality Assurance (QA) Regulatory Compliance Research and Development Research Ethics Standard Operating Procedure (SOP)Required Experience:
Senior IC
About Company
About Johnson & Johnson A t Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 130 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s larges ... View more