Senior (5+ years of experience)
Summary of the Role
We are seeking a highly skilled and experienced Veterinary Drug Development Specialist to lead our efforts in creating innovative pharmaceutical products for veterinary use. The candidate will be responsible for overseeing the entire drug development process from concept to market, ensuring compliance with regulatory standards, and contributing to the advancement of veterinary medicine.
Required Skills
Strong leadership and project management skills.
Excellent communication and interpersonal skills to work effectively with multidisciplinary teams.
Critical thinking and problem-solving abilities.
High level of expertise in veterinary pharmacology and drug development processes.
Ability to analyze and interpret complex scientific data.
Proficiency in relevant software and tools used in drug development and trials.
Qualifications
Doctor of Veterinary Medicine (DVM) degree or equivalent qualification in a related field.
Advanced degree (Ph.D. or equivalent) in pharmacology, toxicology, or a related discipline is highly preferred.
At least 5 years of experience in veterinary drug development or a related field.
Proven track record of successful drug development projects and product launches.
In-depth knowledge of regulatory requirements related to veterinary pharmaceuticals, including FDA, EMA, and other international guidelines.
Responsibilities
Lead and oversee the development of new veterinary drugs, from initial concept through to regulatory approval and market launch.
Design and implement preclinical and clinical trials in collaboration with veterinary teams, ensuring compliance with ethical and legal standards.
Collaborate with cross-functional teams including research scientists, regulatory affairs, and marketing to drive the development process.
Stay updated on industry trends, emerging technologies, and regulatory changes to ensure innovative and compliant drug development.
Mentor and guide junior scientists and development team members in best practices and standard operating procedures.
Serve as a key scientific liaison between the company, regulatory bodies, and other stakeholders.
Contribute to scientific publications and present findings at conferences and industry events.