Sr Manager Nonclinical Safety

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:
Discovery & Pre-Clinical/Clinical Development

Job Sub Function:
Nonclinical Safety

Job Category:
People Leader

All Job Posting Locations:
Beerse, Antwerp, Belgium

Job Description:

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

We are searching for the best talent for a Sr.

Manager Safety Pharmacology, Nonclinical Safety.

Global Safety Pharmacology (GSP) sits within the Translational Sciences (TS) Group in the division of Preclinical Sciences & Translational Safety (PSTS).

Essential Job Duties & Responsibilities


* The Senior Manager is responsible for the line management of the “In Vivo Group”.


* The candidate must have a strong interest in innovative science, drive the integration of AI into our consolidated databases and provide oversight and steer the translational/in silicol DataSciences work within Translational Safety.


* Strong strategic analytical background, having the ability to translate preclinical datasets and processes, data acquisition and management related needs into technical solutions that align with portfolio questions.


* This role will serve as a member of the GSP management team and provide mentorship, tutorship and career development opportunities for GSP & TS team members, where deemed necessary.


* Provide expert scientific support to PSTS project teams as a TS representative on the team.


* In collaboration with other preclinical safety staff members, establish and execute, upon request, local in vivo models/assays & provide global scientific advice in support of PSTS teams including oversight/monitoring of internal in vivo research activities, assuring prioritization of work targeted toward impactful portfolio contributions, keeping the 3R’s (refinement, replacement & reduction) in mind.


* Manage the study monitors of external non-GLP CRO work and act as a study monitor, where necessary


* Maintain awareness of the “Principles of Good Laboratory Practices (GLP)” that can/should be applied in studies, in which involved as an subject matter expert providing input ...