Join a global leader in veterinary pharmaceuticals and take part in a unique human adventure where every contribution shapes the future of animal health.
Animal health is key to the health of the planet.
Working at Virbac means taking part in a unique adventure in which the engagement of every one of us contributes to the business' evolution.
Encouraging internal mobility between positions and countries, offering individual development plans and building a partnership based on trust between our managers and employees are key for Virbac.
We also offer a great work environment that will allow you to explore new territories and balance your professional and personal life.
Finally, fostering engagement also means listening to our people and helping them to acquire new skills, preparing them for the challenges of tomorrow and encouraging them to contribute to an ever more responsible and sustainable approach to our business.
About the Role
As a Clinical Research and Development Associate, you will play a pivotal role in our Research and Development (R&D) team.
Your primary responsibility will be to manage, design, and execute clinical programs that support the development and the registration of new veterinary pharmaceutical and vaccine products.
From planning clinical trials to compiling data for regulatory submissions, your work will ensure that Virbac continues to deliver innovative, high-quality solutions for animal health.
This role is ideal for an experienced clinical researcher with a strong background in veterinary sciences, project management, and regulatory compliance within the animal health industry.
Key Responsibilities
Develop and budget clinical programs to achieve label claims for new products.
Ensure clinical programs comply with local and international regulatory guidelines.
Build and maintain a network of contract research organizations (CROs), veterinarians, and animal health experts.
Design study protocols and manage implementation within budget and timelines.
Monitor study progress and resolve issues promptly.
Write, edit, and approve final study reports.
Propose creative solutions to development challenges and support Go/No-Go decisions.
Serve as a Project Leader when required, driving project success on time and within budget.
Write and compile Efficacy, Safety, and Residue dossiers for regulatory submissions.
Address regulatory deficiencies with prompt, logical responses.
To be successful in this role
Proven ability to plan, manage, and monitor clinical studies to Australian and international standards.
Strong knowledge of the animal health regulatory environment in Australia and New Zealand.
Expertise in GCPv and GLP (veterinary), study design principles, and statistical analysis of biological data.
Experience with pharmacological and vaccine development processes.
Demonstrated project management skills, including risk analysis and budget management.
Excellent research, analytical, and problem-solving abilities.
Proficient in Microsoft Office, Google applications, and technical tools like GraphPad or equivalent.
Familiarity with project management software (e.g., Project Insight).
DVM (Preferred) or PhD in veterinary science
High-level proficiency in written and spoken English, including scientific and technical writing.
Proficiency in French and/or Spanish is considered an asset.
Virbac is an equal opportunity employer who believes diversity of thought, background and experience strengthens relationships and benefits our people, clients, and communities.
We are committed to cultivate an inclusive and high-performing culture where our people thrive and are proud to bring their whole selves to work, inspiring a respectful and inclusive environment.