As Project Leader - clinical study, you are in charge to
You are graduated as a Master degree in Life Sciences, preferably in Immunology. You have a minimum of 2 years of experience in similar position, in biotechnology. You have a good knowledge of clinical study conduct, a good knowledge and understanding of bioanalytical method validation guidelines and requirements. Also, you have knowledge and understanding of GLP, GCLP regulations to carry out GLP studies. You demonstrate knowledge of procedures and protocols for containment of biohazardous material, safety procedures and guidelines. You fluently speak English. Your soft skills are Strong quality mindset, strong cross-functional communication skills, capable of producing document of high quality, rigorous and autonomous in the conduct of their work, effective organizational skills and flexibility and ability to lead a study.
Must accept to perform duties or supervise activities in Bio Safety Level (BSL) 1 or 2 facilities where biological samples may be either naturally or experimentally infected with potentially hazardous virus such as HIV, HCV, or CMV;
Employee is personally responsible for following Health and Safety guidelines/instructions. This position can involve evening and/or week-end work.
A permanent contract is offered for this function with a salary package matching your skills & experience. The opportunity to develop your skills or to evolve within this company is also open.
You're interested in this job? We kindly invite you to apply directly on our website experis.be. Do you have questions? You can contact or 0478/90.63.68.