Associate Director

The Impact You’ll Make

We are seeking an experienced Drug Discovery Toxicologist who will provide project teams with scientific expertise and leadership for the safety assessment of Recursion programs from early discovery, through to candidate selection and beyond. You will contribute to the assessment and selection of novel drug targets and optimisation of novel candidate molecules using innovative molecular, cellular and in vivo technologies to maximise predictive safety science and investigative toxicology.

In this role, you will:

• Represent Toxicology as the Subject Matter Expert on cross-functional project teams within Discovery
• Provide expert input, guidance and strategy on project safety assessments, with a specific focus on discovery projects
• Act as a key resource for early safety assessment during the drug discovery phase, providing scientific knowledge and expertise to cross-functional project teams
• Use established toxicology screening strategies to predict, assess and mitigate target- and drug-related safety risks in support of the drug discovery portfolio
• Refine and implement innovative experimental strategies and use the data to assess and/or provide mechanistic understanding of safety issues
• Collaborate with CROs to ensure best practice for in vitro and/or in vivo safety assessment
• Prepare verbal and written summaries for internal discussions. Work with the Discovery teams to develop optimal strategies to address specific safety issues within the project teams
• Present summary data to project teams, Recursion senior leadership and external partners as needed

The Team You’ll Join 

Reporting to the Head of Toxicology, you will have responsibility for the safety assessment of compounds moving through Discovery and into Development. As the Toxicology subject matter expert, you will work collaboratively with project team members across functions including pharmacology, DMPK and chemistry to support progression of compounds through the portfolio.

The Experience You’ll Need

• DVM, PharmD, PhD in toxicology, Pathology, Physiology, Biochemistry or expertise in related biological scientific disciplines with an emphasis on Oncology/Immunology is preferred. Board Certification in Toxicology (DABT/ERT) is a plus
• 7+ years experience in safety sciences in the Biotech/Pharma industry
• Experience in project team membership as a toxicology representative in a matrix environment
• Experience with in silico and in vitro safety assessment is a must; experience with in vivo safety assessment would be an advantage
• An in-depth knowledge of discovery toxicology, and experience designing and critically evaluating results of exploratory toxicology studies
• Experience of secondary pharmacology assessment would be an advantage
• An understanding of in vitro to in vivo translation of potential toxicities and implications for human safety
• Broad background in novel methods of identifying potential toxicities and developing risk mitigation plans
• Experience with the use of AI tools to predict toxicology endpoints would be an advantage
• Highly motivated scientist, who can work independently, with excellent oral/written communication skills

Working Location & Compensation:

This is office-based, hybrid role can be based in either our New York City or Londonoffice. Employees are expected to work in the office at least 50% of the time. Relocation support can be provided for this role. At Recursion, we believe that every employee should be compensated fairly. Based on the skill and level of experience required for this role, the estimated current annual base range for this role is:

• $182,700 - 229,900 USD for candidates based in the United States 
• £93,500 - £109,700 GBP for candidates based in the United Kingdom 

You will also be eligible for an annual bonus and equity compensation, as well as a comprehensive benefits package.

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