Pharma Clinical development scientist

Pharma Clinical Development Scientist

As a global leader in animal health, Ceva Animal Health is committed to innovative health solutions for all animals, contributing to a sustainable future. We prioritize the well-being of farm animals, companion animals, and wildlife, emphasizing a 'One Health' approach and fostering diversity, equity, and inclusion.

Your Missions:

1. Clinical Development Strategy: Contribute to the development and lifecycle management of new products, ensuring alignment with target profiles and overseeing implementation.
2. Clinical Study Management: Lead and coordinate clinical studies in compliance with GCP, EMA, FDA, and animal welfare standards, including study design, protocol development, and results reporting.
3. Core Team Role: Provide clinical expertise and strategic support within project teams.
4. Cross-functional Collaboration: Work with Innovation, Regulatory Affairs, and other departments.
5. Regulatory Support: Assist in preparing regulatory dossiers and responding to agency inquiries.
6. Technical/Marketing Support: Support product launches with scientific communication.
7. Innovation Support: Conduct proof-of-concept studies.
8. Expertise Development: Build and maintain expertise in relevant therapeutic fields.
9. Network Management: Develop and manage a network of experts.
10. Monitoring: Keep abreast of regulatory and scientific literature.

Context and Challenges: The role involves stakeholder interaction, managing diverse studies, adhering to regulatory standards, and working within an international environment.

Your Profile:

• Veterinary degree or strong scientific background in veterinary medicine, especially internal medicine.
• At least 5 years of experience in veterinary research or product development.
• Experience in pet veterinary practices (preferred).
• Knowledge of clinical trial methodology, GCP, biostatistics, and European regulations.
• Proficiency in clinical project management and CRO management.
• Understanding of EMA and FDA regulatory requirements.
• Strong scientific writing and communication skills.
• Effective project management and team collaboration skills.
• Fluency in English; French skills are a plus.