Professional Toxicologist (Non-Clinical Safety, Hellerup)

Job summary

This role involves managing non-clinical safety assessments and evaluations to support drug development in a biopharmaceutical setting. The position is based in Hellerup, Denmark, and requires collaboration with internal and external stakeholders to ensure compliance with safety and regulatory standards.

Qualifications

• Relevant academic degree, preferably MSc or PhD in Veterinary Medicine, Pharmaceutical Sciences, or related Life Sciences.
• Solid understanding of animal physiology and pathology.
• Experience with GLP is advantageous.
• Strong oral and written communication skills in English.

Responsibilities

• Independently manage non-clinical in vitro and in vivo safety assessment studies in compliance with safety and regulatory requirements.
• Participate in multi-disciplinary project teams to develop and execute non-clinical safety strategies.
• Deliver high-quality non-clinical safety evaluations for programs, including early-stage projects.
• Support regulatory interactions and clinical trials with Non-Clinical Safety input.

Skills

• Strong analytical skills and a structured approach to managing multiple timelines.
• Ability to work collaboratively and establish professional relationships.
• Proactive, self-motivated, and capable of adapting to changing priorities.

Education

• MSc or PhD in Veterinary Medicine, Pharmaceutical Sciences, or other Life Sciences.

Tools

• Familiarity with GLP standards and safety assessment methodologies.