• designing, contracting, coordinating, monitoring and reporting toxicology and safety pharmacology studies for worldwide product registration;
• participating in drug development project teams and communicating the relevance and interpretation of study findings to management;
• preparing relevant sections of regulatory documents;
• demonstrating a high level of proficiency, creativity, collaboration with others and independent thought;
• building effective working relationships throughout the organization to achieve goals;
• maintaining broad knowledge of state-of-the-art principles and theories and possessing advanced knowledge of scientific principles and concepts in field of expertise; and
• proactively contributing to, and demonstrating scientific leadership in, scientific literature and addressing scientific issues.

Requirements:

PhD in toxicology, pharmacology or closely related field and at least 5 years experience in the pharmaceutical industry. Prior experience with CRO interactions is a plus. Ability to integrate toxicity data with pharmacokinetic profiles, and extrapolate non-clinical data to humans. Superior communications, interpersonal and organizational skills are essential, along with computer proficiency.