Senior Toxicology Strategist
4 weeks ago
Transforming Hope into Reality
At Blueprint Medicines, we are seeking a highly skilled Senior Toxicology Strategist to join our Preclinical Drug Safety team. As a key member of our Quantitative Translational Pharmacology (QTP) group, you will play a critical role in developing and implementing toxicology strategies for multi-disciplinary program teams.
Key Responsibilities:
- Develop and lead the general toxicology strategy for Preclinical Drug Safety.
- Navigate compound safety risks through various stages of drug discovery and development, including development candidate (DC) nomination.
- Design, monitor, and interpret toxicology and safety pharmacology data from investigative, non-GLP and GLP-compliant toxicology studies.
- Provide toxicology support for regulatory submissions, including the authoring of nonclinical safety sections of US and international regulatory applications.
Requirements:
- PhD in toxicology, pharmacology, or a related discipline with 8 years postgraduate and/or industry experience.
- Strong understanding of technical principles and basic methodologies for in-vitro and/or in-vivo pharmacology and toxicology in a pharmaceutical setting.
- Demonstrated ability to interpret toxicology data in the context of a compound's pharmacokinetic profile.
- Ability to successfully influence project teams and operate effectively in a matrixed environment.
Why Join Us?
At Blueprint Medicines, we foster a culture of equity, diversity, and inclusion. We are an equal employment opportunity and affirmative action employer, committed to creating a workplace that is welcoming and inclusive for all employees. We believe that a diverse and inclusive workplace is essential to our success and the success of our patients.
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