Johnson & Johnson Careers

Associate Director, Clinical Trials Management - Cardiovascular

Irvine, California
Clinical Trial Administration

Job Description

Requisition ID: 9590170901

Associate Director – Clinical Trials Management /Cardiovascular
The Cardiovascular & Specialty Solutions (CSS) Group, part of the Medical Devices sector within Johnson & Johnson, is recruiting for an Associate Director - Clinical Trials Management/Cardiovascular, located in Irvine, CA.
The CSS Group consists of six diverse businesses including Advanced Sterilization Products (ASP), Biosense Webster (BWI), CNV Neuro, Mentor, and Sterilmed. The CSS Group serves a diverse base of customers in Ear, Nose and Throat (ENT), Infection Prevention, Electrophysiology (EP), Neurovascular and Neurosurgery, Surgical and Non-Surgical Aesthetics, and Reprocessing. 
This individual will be responsible for clinical trial management within the Clinical R&D Operations CoE, as well as fostering strong, productive relationships with colleagues across the organization. Serves as the liaison with the Clinical R&D Franchise for projects under his/her responsibility.
The Associate Director – Clinical Trials Manager will:
• Serve within the Clinical R&D Operations CoE group to execute company sponsored clinical trials for the Medical Device Franchises
• Manage all operational activities of assigned clinical trials/programs within the Clinical R&D Operations group
• Serve as the liaison to the Clinical R&D Franchise and Clinical R&D BSDM for projects/trials/programs under his/her responsibility and may serve as a member of the clinical trial/study/program core team
• Serve as a contact for clinical trial sites
• Solve problems arising during clinical trial execution, and will seek guidance for more complex problems, as needed
• Manage all operational activities of assigned clinical studies within the Clinical R&D Operations group
• 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
• Be involved in other tasks to support Clinical R&D Operations and R&D Clinical Franchise as needed
• Plan, track, and manage assigned projects 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

· Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.
· BS with at least 10 years, MS with at least 8 years, PhD with at least 6 years of relevant experience preferred.
· Minimum of 2 years people management is required.
· Knowledge of Good Clinical Practices(GCP) is required.
· Significant previous experience in clinical project leadership across multiple studies/programs required.
· Experience with budget planning, tracking and control is required.
· Clinical/medical background is preferred.
· Cardiovascular background, preferably with Electrophysiology is preferred.
· Travel up to 20% is required.
· Performs other related duties as required.

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