Johnson & Johnson Careers

Staff Clinical Trial Leader – Cerenovus 1 of 2

Irvine, California
Clinical Trial Administration

Job Description

Requisition ID: 5909180313

Staff Clinical Trial Leader – Cerenovus
Johnson & Johnson’s Cardiovascular & Specialty Solutions (CSS) Group within Medical Devices is recruiting for a Staff Clinical Trial Leader for Cerenovus located in Irvine, Ca. The CSS Group serves a diverse base of customers in Ear, Nose and Throat (ENT), Infection Prevention, Electrophysiology (EP), Neurovascular, Surgical and Non-Surgical Aesthetics, and Reprocessing.
Cerenovus, part of the Johnson & Johnson Medical Devices Companies, is a global leader in neurovascular care. Our commitment to changing the trajectory of stroke is inspired by our long heritage and dedication to helping physicians protect people from a lifetime of hardship. Cerenovus offers a broad portfolio of devices used in the endovascular treatment of hemorrhagic and ischemic stroke.
This individual will be responsible for leading one or several clinical trials within the Clinical R&D Operations CoE, as well as fostering strong, productive relationships with colleagues across the organization. Serves as the trial leader for clinical study execution. 
The Staff Clinical Project Leader will:
· Serve as a Staff Clinical Trials Leader within the Clinical R&D Operations CoE operations group to execute company sponsored clinical trials for the Medical Device Franchises
· Manage all operational activities of assigned clinical studies within the Clinical R&D Operations group
· Serves as a member of the clinical trial/study/program core team and may serve as the liaison with the Clinical R&D Franchise and Clinical R&D BSDM for projects under his/her responsibility
· May serve as the primary contact for clinical trial sites
· Independently solves problems arising during clinical study execution, and will seek guidance for more complex problems, as needed
· Provide internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders
· May be involved in other tasks to support Clinical R&D Operations and R&D Clinical Franchise as needed
· Plan, track, and manage assigned clinical trials/programs budgets to ensure adherence to business plans
· Support the implementation of new clinical systems/processes, and provide support for publications, as needed.
· Interface and collaborate with site personnel, IRBs/ECs, Competent Authorities/MoH, contractors/vendors, and company personnel
· Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance
· Manage resources assigned to designated clinical studies to provide quality deliverables while maintaining optimal efficiency
· Act as an operational expert rotating to new projects to provide technical expertise and training in starting new studies.
· Support Senior CTM or CTM within a large or complex regulated clinical study/program.
· Exhibit proficiency and act as a Subject Matter Expert in clinical trials involving complex design issues. May provide solutions and guidance on complex situations.
· Manage work done by CROs under CTM/Senior CTM guidance.
· Identify and ensure strategies, resources, and accountabilities are in place to achieve rapid, cost-effective, and high quality execution of assigned clinical studies/programs, including those assigned to direct reports.
· Review and provide feedback on clinical operation section of protocols with minimal supervision.

· A minimum of a Bachelor’s Degree is required, preferably in Life Science, Physical Science, Nursing, or Biological Science
· MS or PhD is preferred
· A BS with at least 6 years of experience, MS with at least 5 years of experience, or a PhD with at least 3 year of relevant experience is required
· Previous experience in clinical trial management or equivalent is required
· Experience working with neurovascular is preferred.
· Experience working well with cross-functional teams is required
· Relevant industry certifications are preferred (i.e., CCRA, RAC, CDE)
· Experience managing others is preferred
· Clinical/medical background is preferred
· Medical device experience is preferred
· This position may require up to 30% travel


Primary Location
United States-California-Irvine
Depuy Orthopaedics. Inc. (6029)
Job Function
Clinical Trial Administration
Requisition ID