A full-time member of staff will be employed to carry out in-vivo pharmacology/toxicology analyses in preclinical studies within the scope of the project implemented by the Izmir Biomedicine and Genome Centre.


Duties and Responsibilities :

  • To carry out in-vivo pharmacology/toxicology analyses in preclinical studies,
  • To carry out all procedures of the tests in line with codes of conduct and biosafety rules,
  • To work according to methods and procedures prepared within the GLP requirements,
  • To ensure the compliance of the conditions in the Laboratory Animals Unit (caring, feeding and environmental conditions) and to keep a regular record,
  • To check the health conditions of the animals prior to experiments and ensure they are fit for the test.

Desired Qualifications :

  • University degree from the department of Pharmacy, 
  • Certificate to use laboratory animals,
  • Adequate level of English grammar to follow publications,
  • Open to learning, interested in research, solution and result oriented,
  • Analytical thinking and problem solving abilities,
  • Meticulous, accurate work; competent to carry out business follow-ups,
  • Advanced skills in planning and organisation,
  • No military obligation for male candidates.
Preferred Qualifications :
  • Master’s degree/PhD in Pharmaceutical Toxicology or Pharmacology,
  • Experience in the quality control tests of medicines and in vivo analysis methods.