Clinical Research Associate (Associate Site 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 Support

Job Category:
Professional

All Job Posting Locations:
Beerse, Antwerp, Belgium

Job Description:

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

Johnson & Johnson is currently seeking a Clinical Research Associate (Associate Site Manager) to join our Global Clinical Operations team located in Beerse, Belgium.

One day per week office presence is required.

We are looking for a driven Associate Site Manager to serve as the primary contact point between the Sponsor and the Investigational Site for trials in phases 1b, 2 & 3 in Belgium and in The Netherlands.

As Associate Site Manager, you have to ensure inspection readiness and compliance with the clinical trial protocol, Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations from study start-up through to site closure.

We need a flexible Site Manager who is able to work independently, is a real teammate, a quick learner, a problem solver, and a good communicator.

You will collaborate with a Local Trial Manager (LTM), a Clinical Trial Assistant (CTA), and a Trial Delivery Manager (TDM) to perform trial-related activities for assigned protocols and sites and you are responsible for the overall site management activities.

You will be part of a hardworking, enthusiastic, and committed team of +100 people eager to deliver and helping to improve the lives of millions of patients.

Principal Responsibilities:



* Responsible for activities ranging from site initiation and start-up, over preparation and conduct of site monitoring, oversight of key performance indicators to site/study close-out.


* Responsible for the implementation of a site-level analytical risk-based monitoring model and for working with the site to ensure timely resolution of issues and deviations identified during monitoring visits.


* Contributing to site-level recruitment and retention strategies and implementation of mitigation actions in partnership with other functional areas.


* Att...