Non‑Pharmaceutical Product Clinician
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As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.
We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.
Indeed, Our “Together, Beyond Animal Health” vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.
As part of our “Diversity, Equity and Inclusion” policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.
Your
missions :
Job Overview:
Within the R&D department, and more specifically the Clinical Development Sciences team, the Clinical Development Scientist – Non‑Pharmaceutical Products plays a central role in designing and implementing clinical development plans for products such as dietary supplements (pet food), veterinary care products, and cosmetics.
This position operates in an international environment characterized by a wide variety of studies, complex regulatory requirements, and numerous internal and external stakeholders.
Main Responsibilities:
Actively participate in the design of the non-pharmaceutical product development plan: Work collaboratively within multidisciplinary project teams to integrate clinical data into the non-pharmaceutical product development and innovation strategy.
Define and implement the clinical development plan: Develop, within the project team, the list of studies required to support the development and launch of new products, and coordinate its execution.
Develop study protocols: Design protocols in coordination with regulatory, legal, and marketing departments, ensuring compliance with scientific and regulatory standards.
Plan, implement, and oversee clinical studies and consumer tests: Organize and lead the execution of studies in collaboration with internal teams (biometrics, clinical operations, clinical batches) and external partners (CROs, veterinarians, experts). Ensure data quality, regulatory compliance, animal welfare, and optimization of resources and timelines.
Manage CROs and contracts: Establish contracts with the legal department and ensure operational follow-up with CROs to guarantee quality and adherence to deadlines.
Collect, analyze, and communicate results: Ensure rigor in data collection and analysis. Present results clearly, draft or contribute to study reports, and, when applicable, participate in writing scientific publications or posters.
Ensure compliance with budgets and timelines: Monitor that studies are conducted within the allocated time and budget.
Provide clinical and scientific expertise: Offer expertise to internal teams and, when necessary, contribute to pharmaceutical projects within your area of specialization.
Your
profile :
Qualifications :
Education: Master’s degree, Engineering degree, Veterinary Doctor (DVM), or PhD.
Experience: at least 5 years of relevant experience in the development of veterinary dietary supplements (pet food), nutritional products, etc.
Technical skills: clinical methodology, clinical study protocols, regulatory knowledge, medical writing, project management, and CRO management.
Soft skills: strong organizational skills, scientific rigor, adaptability, teamwork, ability to manage external relationships, and commitment to animal welfare.
Languages : fluent written and spoken English.
Additional information :
Location: hybride position based at the Libourne Campus.
