Principal Scientist, Project Toxicologist

Principal Scientist, Project Toxicologist

Join to apply for the Principal Scientist, Project Toxicologist role at argenx.

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi‑dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first‑in‑class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases.

We are building a new kind of biotech company, one that maintains its roots as a science‑based start‑up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company, our partnerships, our science, and our people, because when we do, we deliver more for patients.

The argenx PharmToxBA team is a functional expert group in the Development organization with expertise in nonclinical safety testing, operations of regulated studies and nonclinical and clinical bioanalytics. We closely work with colleagues from other functional areas and are part of multidisciplinary teams at the heart of argenx discovery and development. argenx works via a strong outsourcing model where scientific and quality oversight from the sponsor is an important part of our work. Our working language is English.

Within the PharmToxBA team we are looking for an experienced Project Toxicologist with demonstrated industry expertise in large molecule drug development. The successful candidate will represent the PharmTox group as a cross‑functional representative in early development projects where they will act as a hands‑on project toxicologist to deliver non‑clinical strategies, studies and submission documents. We expect 4 or more years of relevant experience working in cross‑functional project teams.

Project toxicologists at argenx support the development of our compounds from an early stage (lead optimization) up to submission for marketing and beyond. They are active members of the Early Development teams and late development Asset Teams. They design the nonclinical safety strategy in alignment with our stakeholders and present concepts and results to project teams and senior management. All our studies are conducted in partnerships with leading CRO partners.

At argenx, we highly value co‑creation and collaboration. Frequent personal interactions are central to our work culture.

Project toxicologists can be supported by study monitors and operational specialist for smooth conduct of nonclinical safety studies or they study monitor their own studies, depending on the workload.

The project toxicologist is expected to significantly contribute to the authoring and review of regulatory documents and requests for information.

Responsibilities

• Create early nonclinical safety screening strategies including data generation for the selection of relevant species to ensure smooth transition from discovery to IND‑enabling studies
• Design, development and oversight of nonclinical safety package from IND / CTA through BLA
• Obtain buy‑in from all stakeholders and ensure alignment with project team goals
• Follow up outsourced activities and discuss with experts at the partner companies
• Closely work with argenx study monitor and toxicology team on implementation of strategy, including planning, execution and close out of individual studies
• Ensure compliant execution of studies by study monitoring either in person or with support of study monitor and coordinate contributions of other sponsor disciplines (CMC, Bioanalytics, Pharmacokinetics)
• Collaborate with other scientific disciplines to interpret the study outcomes and present at internal multidisciplinary project teams
• Actively contribute to the development strategy at internal multidisciplinary project / clinical team meetings. Present and discuss work that is under responsibility of the PharmTox team
• Collaborate with medical writer and regulatory affairs in development of regulatory dossiers and the investigator brochure while ensuring nonclinical safety‑related content is correct and comprehensive
• In collaboration with the program manager, ensure correct financial and project planning
• Together with Global Sourcing and Alliance Management and program managers, oversee the timely commission of studies to CRO

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Equal Opportunity

At argenx, all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics. argenx is proud to be an equal opportunity employer.

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