Study Monitor, NIBR Preclinical Safety (NJ or MA) " >Study Monitor, NIBR Preclinical Safety (NJ or MA)

Jun 30, 2021

Job Description

6000! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on new technologies that have the potential to help produce therapeutic breakthroughs for patients.

As a Study Monitor in the Preclinical Safety group within NIBR's Translational Medicine team you will be appointed to each outsourced preclinical study based on relevant technical expertise, designated disease area and/or scientific background knowledge and act as the primary scientific contact for the Study Director at the Contract Research Organization (CRO).

in this role you will be responsible for overseeing the progress of the study and for ensuring that the study is conducted, recorded and reported according to the study protocol. You will also ensure that the study is compliant with the appropriate GLP regulations, Novartis animal welfare policies, CRO in-house standard operating procedures, Novartis expert recommendations (where feasible) and all relevant international regulatory guidelines/regulations. Resolution of study related issues, liaisons with internal experts and informing the appropriate people in a timely manner is pivotal to the performance of this role. The study phases and sample delivery timelines should be strategically overviewed and tracked to ensure that internal contributor reports are delivered to the CRO on time and that the CRO meets its agreed main reporting timelines.

Position can be based in East Hanover, NJ or Cambridge, MA

Diversity & Inclusion / EEO

The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

Minimum Requirements

Minimum requirements :

What you will bring to the role:

Educational qualifications vary depending on experience and time spent in the role and may range from MS to PhD.

Solid scientific background in Toxicology gained in either the Pharmaceutical and/or CRO industry.

2 plus years experience in the role of Preclinical Study Director/Study Monitor and/or experience as a Project Team Member/Representative is preferred. Other routes into the role of Study Monitor are possible.

Preferred experience: Registration and certification with one of the International Toxicology registers.

Why consider Novartis?

769 million. That’s how many lives our products touched in 2020. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?

We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks.

We are Novartis. Join us and help reimagine medicine.
Translational Medicine
East Hanover, NJ
Research & Development
Full Time
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Study Monitor, NIBR Preclinical Safety (NJ or MA)

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