Clinical Research Associate (Associate Site Manager)

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at

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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 & 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.

• Attends regularly scheduled team meetings and training.

• May participate to process improvement and training.

Education and Experience Requirements:

• BA/BS degree in Life Sciences Nursing or related scientific field (or equivalent experience)

• Previous clinical trial monitoring experience (1year) is preferred however other relevant working experiences and skills may be considered by the hiring manager

• Strong proven understanding of GCP local laws and regulations

• Strong IT skills in appropriate software and company systems

• Willingness to travel with occasional overnight stay away from home

• Drivers license B required

• Proficient in Dutch English and French

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