Clinicien produits non-pharmaceutiques (H/F)
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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 :
Within the R&D, specifically the Clinical Development Sciences team, the "Non-Pharma Products" Clinician plays a central
role in the design and implementation of clinical development strategies. He/She actively contributes to the development
of the clinical development plan and oversees the execution of clinical studies and consumer efficacy tests for nonpharma products, dietary supplements, and veterinary cosmetic products.
These studies, conducted according to rigorous protocols, aim to generate robust data to support product claims, while
ensuring compliance with current regulations, animal welfare, and cost and time optimization. In close collaboration with
the marketing teams, he/she provides essential information for product launches.
He/She may also be involved in the development of pharmaceutical products within his/her area of expertise.
The context and challenges of the position are characterized by a large number of stakeholders, a wide variety of studies,
regulatory requirements, and studies conducted in an international context.
Main Responsibilities:
• Planning and Execution of Clinical Studies: Collaborate with internal teams (biometry, clinical operations, clinical
batches) and external teams (CROs, veterinarians, experts) to ensure effective implementation of studies,
according to regulations, scientific standards, and animal welfare.
• Protocol Development: Write or contribute to the creation of study protocols in collaboration with the study
team, the regulatory, legal, and marketing departments.
• CRO Management: Establish contracts with the legal department, supervise CROs with regular operational
contact to ensure quality and meet deadlines.
• Data Collection and Analysis: Ensure rigor in data collection and analysis.
• Communication and Interpretation of Results: Clearly present results orally and in writing, write or contribute to
the study report, and if applicable, participate in writing publications or scientific posters to support product
claims.
• Cost Optimization and Deadline Compliance: Ensure studies are conducted within the allotted time and budget.
• Project Team Contribution: Work synergistically with multidisciplinary project teams to integrate clinical data
into product development and innovation strategy.
• Expertise and Support: Provide clinical and scientific expertise to internal teams and contribute to the overall
product development strategy
Your
profile :
• Education: Master's degree, Engineering degree, Veterinary Doctorate, or University Doctorate.
• Experience: Experience in managing clinical trials in the veterinary, dietary supplements, and/or
cosmetics sectors.
• Technical Skills: Clinical methodology, research protocol, consumer testing, medical writing,
regulations, and CRO management.
• Personal Qualities: Organizational skills, scientific rigor, adaptability, teamwork, external relations
management, and concern for animal welfare.
• Languages: Fluent written and spoken English