Director Toxicology

Green Life Science; Glasgow; Hybrid; GBP 100,000 - 125,000; Full time

Job summary

A biotechnology firm is seeking an experienced Associate Director in Drug Discovery Toxicology who will provide scientific leadership across early discovery programs. The ideal candidate will guide project teams on safety assessments and candidate selection. This hybrid position requires an advanced degree in Toxicology or related field and at least 7 years of industry experience. You will be responsible for designing toxicology studies and collaborating with CROs to ensure high-quality safety data, with competitive compensation and benefits offered.

Benefits

Competitive salary

Bonus

Equity

Benefits

Qualifications

• Advanced degree in relevant field with oncology/immunology focus preferred.
• 7+ years of experience in safety sciences (biotech/pharma).
• Strong background in safety assessment techniques.

Responsibilities

• Act as the Toxicology expert on cross-functional project teams.
• Advise on early safety strategy and assessment of novel compounds.
• Design and interpret exploratory toxicology studies.
• Collaborate with CROs for high-quality safety data.
• Present findings to internal teams and stakeholders.

Skills

Toxicology expertise

Safety assessment

Cross-functional collaboration

In vitro assessment

In silico assessment

Education

Advanced degree (DVM, PharmD, PhD) in Toxicology, Pathology, or Biochemistry

Job description

Associate Director, Drug Discovery Toxicology

Location : Hybrid with flexible office requirement

We’re seeking an experienced Drug Discovery Toxicologist to provide scientific leadership across early discovery programs. You’ll guide project teams on safety assessments, candidate selection, and risk mitigation using in vitro, in silico, and in vivo approaches.

Key Responsibilities

• Act as the Toxicology expert on cross‑functional project teams.
• Advise on early safety strategy and assessment of novel compounds.
• Design and interpret exploratory toxicology studies.
• Collaborate with CROs for high‑quality safety data.
• Present findings to internal teams and stakeholders.

Qualifications

• Advanced degree (DVM, PharmD, PhD) in Toxicology, Pathology, Biochemistry, or related field. Oncology / immunology focus preferred.
• 7+ years industry experience in safety sciences (biotech / pharma).
• Strong background in in vitro and in silico safety assessment; in vivo experience a plus.
• Excellent communication and cross‑functional collaboration skills.

Working Model & Compensation

• Hybrid role, some office requirement
• Competitive salary, bonus, equity, and benefits.

This is an opportunity to shape early‑stage drug discovery through innovative and predictive safety science.