Clinical Project Manager

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 jnj.com 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 Operations Job Sub Function: Clinical Trial Project Management Job Category: Professional All Job Posting Locations: Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America Job Description: 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 Clinical Project Manager in Spring House, PA, Raritan, NJ or Titusville, NJ. 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. 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. 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 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 trial governance documentation. Provide support for team-based reporting (i.e., the PLW team list). Additional Responsibilities May Include Mentor and support onboarding of new team members, particularly those in Trial Management. Foster employee engagement, inclusion, and Credo Behaviors.

Requirements Required Minimum Education BS degree or equivalent, preferred areas of study include Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy) Required Years of Related Experience Minimum of 4 years of experience in Pharmaceutical, Healthcare or related industries. Required Knowledge and Experience Strong Project Management experience (preferably in clinical trial management). 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 are essential to this position. Operate and execute with limited supervision. Experience mentoring/coaching others. Ability to support and participate in the hiring, training, development, and evaluation of staff on a regular basis. Strong project planning/management, communication and presentation