Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
Post : Principal Scientist - Toxicology
Summary
About the role The Preclinical Safety (PCS) department within the Novartis Biomedical Research Translational Medicine Unit provides world class preclinical safety profiling and assessment for optimal drug discovery, development and commercialization, with state-of-the-art regulatory compliance. As a Preclinical Safety Profiling Expert, you will join our global PCS team to help us to unleash the power of early safety screening and profiling approaches for advancing translational safety assessment and to drive drug discovery and development. You will bring your curious, innovative, and collaborative mindset to leverage a wealth of non-clinical safety-related data generated within our department and deploy state-of-the-art laboratory science and data exploration methods to accelerate the advancement of innovative medicines.
Key Responsibilities
• Design and implement the early safety screening & profiling strategies, including those associated with secondary pharmacology, genetic toxicology and cardiovascular safety, in collaboration with internal and external partners.
• Give to early ADME-Tox data unification, harmonization, curation, and augmentation to support the Predictive Safety Strategy
• Effectively communicate with customers, including experimental design, data quality, timeline requirements and flowchart planning.
• Understand and implement agreed business strategy defined by local and global Preclinical Safety Profiling requirements, help to lead budget, ensuring appropriate coordination of projects.
• Participate in cross-functional early safety screening & profiling collaborations with Novartis Biomedical Research partners to support the early derisking of compounds, drug targets, and therapeutic modalities
• Deliver clear and concise presentations for audiences with different expertise
• In collaboration with cross-functional partners, provide scientific and strategic input to support the early derisking of compounds, drug targets, and therapeutic modalities
• Ensure quality and compliance of data generation, analyses and resultant reports
Candidate Profile
• PhD with 2+ years or MVSc/MS/M.Pharm with 6+ years of relevant work experience in pharmacology / toxicology
• Understands the basic concepts of hazard identification and risk assessment associated with drug ADME, off-target mitigation, genetic toxicology, and cardiovascular safety.
• Familiar with early drug discovery processes
• Experience with data integrity and quality assurance practices.
• Excellent communication skills and ability to translate analytical concepts for diverse audience and collaborators (English is our primary language
Additional Information
Qualification : PhD with 2+ years or MVSc/MS/M.Pharm with 6+ years
Location : Hyderabad
Job ID : REQ-10004609
End Date : 20th June 2024
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