Study Monitor – Principal Scientist, Translational Medicine, Preclinical Safety

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🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $119.7k - $222.3k / year

⏰ Full Time

🔴 Lead

🧬 Research Scientist

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Novartis

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1996

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Pharmaceuticals • Biotechnology • Healthcare Insurance

Novartis is an innovative medicines company dedicated to reimagining medicine to improve and extend people’s lives. With a presence in over 250 million patients worldwide, Novartis focuses on harnessing scientific breakthroughs to develop transformative, high-value treatments in areas such as cardiovascular, renal and metabolic diseases, immunology, neuroscience, and oncology. The company is committed to diversity, equity, and inclusion, and aims to create a positive impact through societal contributions and environmental sustainability efforts. Furthermore, Novartis engages in research collaborations and embraces modern technology platforms to advance their research and development capabilities, making them a leader in the global healthcare industry.

📋 Description

• Formulates and leads/co-leads novel projects with team or enables matrix collaboration on project/technology solutions to achieve creative results for impact on BR goals • Generates innovative ideas within own team and/or project team/functional community to meet new technical requirements and/or answer project key scientific/technical/development questions • Establishes target dates and priorities to enable data-driven advancements in project teams, within own team, and with collaborators, or within functional community • Oversees the progress of the study and for ensuring that the study is conducted, recorded and reported according to the study protocol • Ensures 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

🎯 Requirements

• PhD or MVSc/MS/M.Pharm with 7+ years of experiences in drug discovery and/or development, preferably as Study Director or Study Monitor in the early preclinical screening and GLP studies • In-depth knowledge of toxicology assays in early development, Safety pharmacology and genotoxicity • Proficient with full range of techniques used in job and core areas • Working knowledge of tools and processes used in drug design and development • Registration and certification with one of the International Toxicology regulations

🏖️ Benefits

• Comprehensive benefits package • Health, life and disability benefits • 401(k) with company contribution and match • Generous time off package including vacation, personal days, holidays and other leaves