Study Monitor – Principal Scientist, Translational Medicine, Preclinical Safety
Location
United States
Posted
2 days ago
Salary
$119.7K - $222.3K / year
Seniority
Lead
Job Description
Study Monitor – Principal Scientist, Translational Medicine, Preclinical Safety
Novartis
• 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
Job 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
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