Full-Time Senior Principal Scientist - Pharmacology/Toxicology

Ensure the role of Pharmacology and Toxicology expert. Involved in early-stage projects (pre-projects), propose actions to evaluate and select them, participate proactively in the conception of project development plans and define the rationale, evaluate acquisition opportunities, assess scientific communications, and give guidance and support for different studies. Support Vetoquinol’s global strategy. Represent the Preclinical and Clinical Department within the Project Team, as a Project Team Member. Coordinate and ensure implementation of the defined actions for product development. These actions must comply with the Target Product Profile, external constraints (regulations, customer expectations), and internal constraints (resources and deadlines).

As an Expert in Pharmacology and Toxicology, you will:

• Establish strategic recommendations in support of pre-projects in your field of expertise.
• Recommend essential studies to confirm interest/validity of selected pre-projects, contribute to their experimental design, analysis, and interpretation of the results.
• Participate in evaluating development opportunities (due diligence) and establish recommendations.
• Contribute to the evaluation of research program opportunities and make recommendations.
• Contribute to the definition of the development plan for Safety and Efficacy sections, in terms of studies and resources.
• Advise and support Study Managers in the conception and design of pharmaco-tox studies.
• Establish the strategy to answer questions within the Pharmacology and Toxicology fields, both internally and externally.
• Participate in the resolution of technical or experimental problems.
• Set up/animate and maintain a network of experts/researchers in Pharmacology and Toxicology.

As a Project Team Member, contribute to the projects:

• Define and propose the development plan for Safety and Efficacy sections.
• Coordinate the actions of the development plan within the Preclinical and Clinical Department.
• Ensure they are executed within the defined time, coordinate corrective actions.
• Keep the Project Team informed.
• Ensure communication and flow of information between the Project Team and Team Managers.
• Contribute to the transcription of desired attributes of the Target Product Profile into target SPC.

You will also contribute to:

• Scientific Communication inside and outside the Vetoquinol Group.
• Scientific Intelligence.
• Group Image and Innovation.
• Participate in/lead working groups of multidisciplinary experts.
• Participate in conventions and monitor scientific literature.
• Represent and defend the Group at professional organizations.

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