Function
R&D Operations
Sub function
Clinical Trial Support
Category
Experienced Analyst, Clinical Trial Support (P5)
Location
North Ryde / Notting Hill, / Australia
Date posted
Jun 13 2025
Requisition number
R-018563
Work pattern
Field-based
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 DESCRIPTION:

• One of the strongest and innovative drug pipelines in industry
• Great Place to Work® Certified - 2024
• Competitive salary package, flexible work practices, award winning benefits
• Continuous training and development
• Open to be based in Sydney, Melbourne, Brisbane, Adelaide and Perth

RESPONSIBILITIES

Our current area of focus is Oncology/Haematology, Infectious Diseases & Vaccines, Immunology, Cardiovascular Disease, and Neurosciences. In GCO, the Senior Site Manager is the sponsor’s interface with the investigative site and a member of the local study management team. The Site Manager covers all aspects of site management from pre-trial assessments through to database locks and close out activities.

This role requires someone with strong communication skills and customer focus. As an exceptional team player, you will liaise and build strong working relationships with internal and external customers, support the implementation of new systems/processes and ensure the smooth running of our projects at your assigned trials sites. In addition, we look for the following attributes in our team – Collaboration, learning agility, resilience, change management, agile approach. Other requirements include:

• BA or BS Degree in Science, Nursing or Life Sciences.
• 3 + years on site experience of clinical trial monitoring experience is preferred
• Demonstrated success as a CRA.
• Excellent communication and problem-solving skills.
• Strong working knowledge of company SOPs, local laws and regulations and assigned protocols.
• Strong knowledge of GCP and local regulatory guidelines.
• Proficient in using appropriate IT software applications and company systems.
• Willingness to travel