Job Description

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: High Wycombe, Buckinghamshire, United Kingdom
:
We are searching for the best talent for our Sr. Specialist, Clinical Project Management (3 positions) to be based in High Wycombe, United Kingdom.
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-041928
Belgium - Requisition Number: R-043230
United Kingdom- Requisition Number: R-043231
Switzerland- Requisition Number: R-043233
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
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
Purpose: The Sr. Specialist, Clinical Project Management is responsible for the creation and management of the integrated project schedule in Planisware. They will collect, consolidate and report budget, timeline and FTE actuals vs. plan and will identify potential issues for the trial(s) through active management of the study schedule.
You will be responsible to:

• Create, manage, and maintain integrated study schedule in Planisware (PLW) including creation of KEMs, Roadmaps, based on planning in PLW.
• Assure 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 and analyzing situational operational scenarios.
• Collect, consolidate, and report financial, timeline and resource data for governance approvals and external funding partnerships. Manage scope control reporting, and FTE/OOP variances.
• Ensure key decisions, actions, risks, issues, lessons learned, and trial governance is reflected in the integrated trial plan in PLW.
• Provide support for team-based reporting (i.e., the PLW team lists).
• Translate operational strategy into PLW and translate PLW output back to the study team.
• Foster employee engagement, inclusion, and Credo Behaviors.

Qualifications/Requirements:
Education:

• BS degree or equivalent, preferred areas of study include Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy). (Required)

Experience:

• Minimum of 4 years of experience in Pharmaceutical, Biotechnology, Healthcare or related industries. (Required)
• Strong Project Management experience (preferably in clinical trial management). (Preferred)
• Experience leading without authority and in muti-functional matrixed and global environments. (Preferred)
• Excellent analytical skills and exposure to financial management are important to this position. (Preferred)
• Operate and execute with limited supervision. (Preferred)
• Ability to support and participate in the hiring, training, development, and evaluation of staff on a regular basis. (Preferred)
• Knowledge of Clinical Research Operations with 2-3 years of exposure to multiple aspects of the execution of global clinical trials (Phases I-IV) (Preferred)

Other:

• Travel up to 10% of the time, defined by business needs.

#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)

Skills Required