Scientist II/Investigator I

Job Summary

As Senior toxicologist, this role is responsible for developing the toxicology strategy of assigned programs. Further, the incumbent will be responsible for the design, adequate budgeting and monitoring of non-clinical safety studies conducted internally and externally both in a GLP and non-GLP environment followed by the interpretation, communication and reporting of non-clinical safety data generated and liaise closely with global cross-functional project teams and interact with regulatory health authorities and external experts.

Oversee and manage toxicology programs along clinical development up to marketing with limited supervision. Plan, monitor, analyze and report preclinical pharmacology and toxicology studies conducted internally or in collaboration with external contract research organizations (CROs) for selected projects.

Serve as function’s representative across R&D projects across therapeutic areas, Manage and coordinate internal and external toxicology studies as part of global teams and take responsibility as preclinical project lead for selected research or development projects.

Owns primary authorship of some nonclinical documents (e.g. protocols, reports). Support the preclinical evaluation of external assets and in-licensing opportunities. Support improvement initiatives to enhance efficiency and quality of the group's deliverables.

• Master’s Degree in Science plus 3+ years
• Ph.d. in Science plus 0+ years’ experience is highly preferred
• Industry experience includes: biotechnology or pharmaceutical industry OR where relevant, biomedical research organization
• Thorough understanding of drug development processes, advanced knowledge of ICH/GLP.
• Demonstrated ability to lead cross-functional, multicultural and international teams.
• Ability to work independently with limited supervision.
• Ability to understand difficult and complex problems.
• Excellent communication and analytical skills.
• Experience in analyzing and presenting research results to scientific and professional audiences.
• Demonstrated planning and organizational skills.
• Ability to work successfully in a matrix organizational structure.
• Proven negotiation skills and ability to identify and engage internal and external expertise as needed.

• Toxicology training highly preferred.
• Experience in medical/regulatory writing desired

Our Benefits

Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join Seqirus.

Seqirus is part of CSL Limited (ASX: CSL). As one of the largest influenza vaccine providers in the world, Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. Learn more about Seqirus.

As a global organisation with employees in 35+ countries, CSL embraces diversity, equity and inclusion. Learn more about Diversity, Equity & Inclusion at Seqirus.