Alizé Pharma, a biopharmaceutical company specialized in the research and development of innovative therapeutics for the treatment of metabolic diseases and cancer, based in the Lyon area, France (69) has currently a great opportunity for:

A Pharmacologist, Preclinical development

• In collaboration with CROs and/or academic scientists, designs and monitors studies in toxicology, pharmacology and other discipline as they relate to preclinical assessment of safety and efficacy.
  
• Leads the preparation of the scientific rationale, study protocols, analysis and interpretation of study results and creation of study reports.
  
• Supervises CROs and ensures all operational study deliverables are met according to timelines, budget, operational procedures and quality standards.
  
• Writes and/or critically reviews scientific abstracts and manuscripts for publication.
  
• Writes and/or critically reviews relevant sections of regulatory documents as applicable (investigators’ brochure, Briefing package, IMPD, IND, CTA, etc…)
• Critically reviews scientific literature and communicates relevant information to colleagues and management.

• PhD in toxicology, pharmacology, or other relevant scientific area, or equivalent combination of education (MD, DVM, PharmD) and drug development experience.
  
• 3 to 7 years of preclinical development experience in the biopharmaceutical industry (Pharma, Biotech, CRO), preferably in recombinant proteins.
  
• Experience in designing, executing, monitoring, and reporting non-clinical studies.
  
• Knowledge of GLP regulations, including writing SOPs and study reports.
  
• Knowledge of regulatory processes.
  
• Autonomy and initiative, good communication skills and team spirit.
• Fluency in English, excellent written skills in both French and English.
• Good practice of the standard software equipment (Word, Excel, Powerpoint, Outlook…).

Alizé Pharma SAS
15, chemin du Saquin
Espace Européen, Building G
69 130 ECULLY
FRANCE

contact@alz-pharma.com