Preclinical Research Expert

About the role

The Emirates Drug Establishment (EDE) is looking for a senior Preclinical Research Expert to lead and advise on pre‑clinical studies that support pharmaceutical and biomedical product development in the UAE. The role bridges laboratory science, regulatory compliance, and strategic planning to ensure high‑quality evidence for clinical translation.

Key responsibilities

• Provide strategic guidance on preclinical research design, execution, and evaluation.
• Review pharmacology, toxicology, and safety studies to ensure alignment with GLP and international standards.
• Assess the robustness, relevance, and quality of preclinical data for regulatory decision‑making.
• Support the translation of preclinical findings into clinical development plans.
• Collaborate with internal teams, external laboratories, academia, and regulatory stakeholders.
• Contribute to building EDE’s scientific and regulatory capabilities.

Required profile

• Advanced degree (PhD, PharmD, MD, MSc or equivalent) in Pharmacology, Toxicology, Pharmaceutical Sciences, Biomedical Sciences or related field.
• Extensive experience in pharmaceutical/biomedical preclinical research, including toxicology and pharmacology.
• Deep knowledge of GLP requirements and international regulatory standards.
• Understanding of the full drug development lifecycle from preclinical to clinical phases.
• Experience with major regulatory authorities or R&D environments is a plus.
• Familiarity with alternative/non‑animal methodologies and emerging preclinical approaches.

Required skills

• Toxicology
• Pharmacology
• Study design
• Good Laboratory Practice (GLP)
• Regulatory affairs
• Non‑animal preclinical models