Job Description

• Define and oversee Toxicology and Non-Clinical Pharmacology strategies for assigned projects.
• Account for Toxicology and Non-Clinical Pharmacology modules in regulatory documents.
• Manage preclinical safety studies in CROs and ensure translational aspects are integrated.

Qualifications:

• PhD, DVM, or equivalent with minimum 5 years of experience as a project toxicologist.
• Experience with biologics and small molecules required; gene therapy or combination drugs a plus.
• Board certification such as DABT/ERT preferred.
• Extensive regulatory toxicology experience and solid understanding of drug development process.
• Excellent communication and presentation skills, with fluency in English.
• Strong problem-solving ability and analytical mindset.

Why Join Us?:

• Empower every person to make a difference for rare disease in a global company with over 1,900 employees.
• Be part of a culture that values Care, Ambition, Urgency, Ownership, and Partnership.
• Enjoy a competitive total rewards package in a team dedicated to innovation.

Sobi

A biopharmaceutical company dedicated to developing innovative therapies for rare diseases. With over 1,900 employees in more than 30 countries, Sobi fosters a culture of inclusion and empowerment.

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