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Associate Director, Drug Discovery Toxicology

Recursion

City Of London

Hybrid

GBP 93,000 - 110,000

Full time

Today
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Job summary

A leading TechBio company in London seeks an Associate Director of Drug Discovery Toxicology. This role involves providing scientific leadership and expertise for safety assessments, collaborating across functions, and ensuring optimal project outcomes. Candidates should have extensive experience in safety sciences and project team leadership in the Biotech/Pharma sector. An attractive compensation package including bonuses and equity is offered for this critical position.

Benefits

Annual bonus
Equity compensation
Comprehensive benefits package

Qualifications

  • 7+ years of experience in the Biotech/Pharma industry.
  • Experience in safety assessment and project teams.
  • Understanding of drug discovery toxicology.

Responsibilities

  • Lead safety assessments for drug discovery projects.
  • Act as subject matter expert in project teams.
  • Communicate findings to internal teams and executives.

Skills

Safety sciences knowledge
Project team experience
Communication skills
AI tools usage

Education

DVM, PharmD, or PhD in related fields

Tools

In silico assessment tools
In vitro assessment techniques
Job description
Associate Director, Drug Discovery Toxicology

London, England; New York, New York

Overview

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.

Responsibilities
  • 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
Team & Collaboration

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 related disciplines with emphasis on Oncology/Immunology; Board Certification in Toxicology (DABT/ERT) is a plus
  • 7+ years of 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; in vivo safety assessment would be an advantage
  • In-depth knowledge of discovery toxicology and experience designing and critically evaluating exploratory toxicology studies
  • Experience of secondary pharmacology assessment would be an advantage
  • 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 and written communication skills
Working Location & Compensation

This is an office-based, hybrid role based in either our New York City or London office. Employees are expected to work in the office at least 50% of the time. Relocation support can be provided for this role. Based on the skill and level of experience required, 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.

#LI-EP1

The Values We Hope You Share
  • We act boldly with integrity. We are unconstrained in our thinking, take calculated risks, and push boundaries, but never at the expense of ethics, science, or trust.
  • We care deeply and engage directly. Caring means holding a deep sense of responsibility and respect - showing up, speaking honestly, and taking action.
  • We learn actively and adapt rapidly. Progress comes from doing. We experiment, test, and refine, embracing iteration over perfection.
  • We move with urgency because patients are waiting. Speed isn’t about rushing but about moving the needle every day.
  • We take ownership and accountability. Through ownership and accountability, we enable trust and autonomy—leaders take accountability for decisive action, and teams own outcomes together.
  • We are One Recursion. True cross-functional collaboration is about trust, clarity, humility, and impact. Through sharing, we can be greater than the sum of our individual capabilities.

Our values underpin the employee experience at Recursion. They are the character and personality of the company demonstrated through how we communicate, support one another, spend our time, make decisions, and celebrate collectively.

More About Recursion

Recursion (NASDAQ: RXRX) is a clinical stage TechBio company leading the space by decoding biology to radically improve lives. Enabling its mission is the Recursion OS, a platform built across diverse technologies that continuously generate one of the world’s largest proprietary biological and chemical datasets. Recursion leverages sophisticated machine-learning algorithms to distill from its dataset a collection of trillions of searchable relationships across biology and chemistry unconstrained by human bias. By commanding massive experimental scale — up to millions of wet lab experiments weekly — and massive computational scale — owning and operating one of the most powerful supercomputers in the world, Recursion is uniting technology, biology and chemistry to advance the future of medicine.

Recursion is headquartered in Salt Lake City, where it is a founding member of BioHive, the Utah life sciences industry collective. Recursion also has offices in Toronto, Montréal, New York, London, Oxford area, and the San Francisco Bay area. Learn more at www.Recursion.com, or connect on LinkedIn.

Recursion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected under applicable federal, state, local, or provincial human rights legislation. Accommodations are available on request for candidates taking part in all aspects of the selection process.

Equal Opportunity Employment Information (Recursion)

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