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Toxicology Strategist

2 months ago

Cambridge, Cambridgeshire, United Kingdom Blueprint Medicines Full time
Transforming Hope into Reality

We are seeking a highly skilled Toxicology Strategist to join our Preclinical Drug Safety team at Blueprint Medicines. As a key member of our Quantitative Translational Pharmacology (QTP) group, you will play a critical role in helping us advance the research pipeline by leveraging your toxicology expertise.

Key Responsibilities
  • Develop and implement toxicology strategies for multi-disciplinary program teams
  • Collaborate with stakeholders within and outside of QTP to facilitate line of sight from research to early development
  • Provide technical expertise and bring a sense of urgency to help project teams advance the Blueprint portfolio and deliver differentiated therapies to patients
  • Help preclinical project teams navigate compound safety risks through various stages of drug discovery and development
  • Design, monitor, and interpret toxicology and safety pharmacology data from investigative studies
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
  • Strong interpersonal, collaborative, and scientific communication skills
About Us

At Blueprint Medicines, we foster a culture of equity, diversity, and inclusion. We are a proud Equal Employment Opportunity and Affirmative Action employer, committed to creating a workplace where everyone feels valued, respected, and empowered to succeed.