Transpharmation is a dynamic preclinical contract research organization that specializes in high-quality, translational drug discovery services. The company provides a friendly and team-oriented work atmosphere as well as competitive wages and benefits.
We’re seeking a motivated Scientific Director to join our dynamic team. In this pivotal role, you’ll lead the design, conduct, and reporting of research studies that support the development of novel therapeutics for human and animal health.
The Scientific Director (SD) is the primary individual responsible for the management and integrity of the design, conduct, and reporting of a research project and for managing, monitoring and ensuring the integrity of Sponsor relationships. The SD is charged to conduct objective research that generates independent, high quality, and reproduceable results. Additionally, the SD is responsible for the direction and oversight of regulatory compliance, compliance with Transpharmation and Sponsor policy, financial, personnel, and other related aspects of the research project.
The SD will have a solid understanding of each individual’s roles and responsibilities within the company and within research studies. The SD will also be involved in business development working closely with the VP of the department, Chief Scientific Officer and Business Development teams.

EDUCATION

• Veterinary or graduate level science degree or B.Sc. degree in a relevant field (e.g., Pharmacology, Pharmacokinetics, Veterinary Sciences, Biochemistry) with at least 3 years of direct experience

EXPERIENCE

• 3-5 years’ experience managing projects, research activities, and collaborative initiatives in a science delivery environment.
• Demonstrated experience and comfort in managing animal studies.
• Experience in the delivery of diagnostic or reference laboratory services under a system of quality.
• Experience in planning and managing human and financial resources.
• Experience in managing communications and high-level preparation of study related documentation.
• Experience conducting safety and efficacy studies.
• Experience handling confidential laboratory and scientific data
• Experience executing administrative strategies
• Proven organizational skills and attention to details
• Demonstrated ability to communicate effectively orally and in writing

KNOWLEDGE

• Knowledge of the principles of biology, pharmacology, chemistry
• Knowledge of the principles of safe handling of potentially pathogenic substances and contaminated materials
• Knowledge of CCAC and OMAFRA regulations
• Familiar with the following acts and regulations: ISO Guide 17025 (1990) and GLP (both Code of Federal Regulations and OECD guidelines).
• Knowledge of occupational health and safety practices
• Knowledge of the principles of scientific research
• Knowledge and understanding of Transpharmation’s Standard Operating Procedures
• Knowledge of computers, including word processing, spreadsheets and databases
• Knowledge of therapeutic development regulatory guidelines.
• Familiar with development of new products for human and animal health care.