Animal clinical study researcher

Location: León

Overview of functions

Coordination of all stages of an animal study (proof of concept, clinical or preclinical trial, post-authorisation study) within the R&D Department.

Specific responsibilities

• Planning and design of animal trials (as sponsor, monitor, investigator or study director)
• Monitoring and operational coordination of animal studies (on-site visits to CROs, farms, etc.), both nationally and internationally.
• Organization and coordination of teams
• Regulatory and ethical compliance management (3Rs) and study quality management (GLP, GCP)
• Drafting and reviewing study protocols and reports, as well as standard operating procedures (SOPs). Análisis y presentación de resultados.
• Management and organization of animal study samples

Requirements

Education: Health Sciences (preferably Veterinary Science/Biology or similar)

Languages: Advanced English (spoken and written)

Experience: (years/area): + 2 years in a similar position in the pharmaceutical industry.

Technical knowledge:

• Knowledge of GLP and GCP studies in different animal species (swine, ruminants and companion animals).
• knowledge of the European Pharmacopoeia and regulatory framework for the registration of veterinary medicines,
• Training Animal experimentation

Personal skills:

Coordination and working in a team with different projects and centres, organisation and planning, attention to detail and data analysis skills.

Other requirements:

• Willingness to travel (nationally and internationally)
• Driving licence