Lead Local Trial 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 https://www.jnj.com

Job Function:
R&D Operations

Job Sub Function:
Clinical Trial Project Management

Job Category:
Professional

All Job Posting Locations:
Adelaide, South Australia, Australia, Eight Mile Plains, Queensland, Australia, North Ryde, New South Wales, Australia, Notting Hill,, Victoria, Australia, Osbourne Park, Western Australia, Australia

Job Description:


* Great Place to Work® Certified - 2024


* Competitive salary package, flexible work practices, award winning benefits


* Continuous training and development

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

THE OPPORTUNITY

An opportunity is now available for a Senior Clinical Project Manager/Lead Local Trial Manager to join our high performing Global Clinical Operations (GCO) team.

The Lead, Local Trial Manager plays a crucial role in overseeing the local management of clinical trials within Australia.

You will be your global project team’s local point of contact and will provide local project team oversight to achieve flawless execution of your assigned clinical trials.

You will work closely with your Manager, Clinical Operations, however you will remain responsible for the conduct of your projects.

You will cover all aspects of study execution from feasibility and pre-trial assessment through to database lock and close-out activities.

The role extends more broadly to include, in some cases, leading a cross functional team or working on early development pipeline products.

As an exceptional leader, you will build strong working relationships with internal and external customers and ensure the smooth running of our trials; delivering them on time, on budget and in accordance with Good Clinical Practice (GCP), relevant SOPs and regulatory requirements.

In addition, you will be required to contribute to process improvement as well as training and mentoring other team members.

The is a permanent, full-time role.

RESPONSIBILITIES


* Lead country protocol and site feasibility assessments in collaboration with relevant stakeholders, ensuring adherence to local...