Regulatory Affairs Scientist (Contract)
New Today
As a Scientific Study Monitor, you will join our PCS team to oversee non-clinical research activities across multiple projects and disease areas, focusing on in-vivo toxicity and/or in-vitro screening toxicity studies conducted at our CRO partner sites. You will act as the primary scientific contact for the Study Director.
Lead or co-lead novel projects, facilitating collaboration to achieve impactful results aligned with BR goals. Generate innovative ideas to meet new technical requirements and address key scientific questions.
# Serve as the appointed Study Monitor for outsourced preclinical studies, based on expertise and scientific background, acting as the primary contact for the Study Director at CROs.
# Oversee study progress, ensuring conduct, recording, and reporting comply with the protocol, GLP regulations, animal welfare policies, and international guidelines.
# Maintain knowledge of HA regulations (Swiss medic, OECD, FDA) to support GLP toxicology studies.
# Potentially serve as a part-time PCS PTM.
PhD or MVSc/MS/M.Deep knowledge of toxicology assays, safety pharmacology, and genotoxicity.
Excellent communication skills, strong teamwork, and logistical planning abilities.
Registration and certification with an International Toxicology register.
Why Novartis: Our purpose is to reimagine medicine to improve and extend lives. Commitment to Diversity and Inclusion: We strive to build an inclusive, diverse work environment reflecting the communities we serve.
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Help us create breakthroughs that change patients lives. Join our community of passionate professionals.
Discover how we support your personal and professional growth:
Animal Models, Bioinformatics, Chemistry, Clinical Research, Collaboration, Communication, Data Analysis, Drug Development, Drug Discovery, Ethics, Flexibility, Influencing Skills, Laboratory, Lifesciences, Medical Research, Patient Care, Pharmaceutics, Problem Solving, Regulatory Compliance, and more.
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- Location:
- London
- Job Type:
- FullTime