PFor over 50 years, the ERBC Group has established itself as a key international partner as a Contract Research Organization (CRO) for pharmaceutical, biotechnological, and chemical companies specializing in the safety evaluation of innovative drugs (pharmacology and toxicology) and chemical compounds. Arising from a strategic merger between two CROs located in Pomezia (near Rome) and Baugy (near Bourges) in 2019, ERBC has since broadened its horizons through various organic growth initiatives and multiple mergers and acquisitions. /ppComprising ERBC (non-clinical evaluation), Voxcan (preclinical medical imaging in oncology, infectiology, osteoarticular), OncoFactory (preclinical and clinical evaluation in oncology), Novaxia (histopathology and pathology), and Bioprim (accommodation and breeding of non-human primates), the Group develops a range of unique services from preliminary stages in "Discovery," regulatory stages to entry into the clinical phase to ensure the best chances of success for the RD projects of our clients. /ppDedicated to patients' health, the ERBC Group combines exceptional scientific and technical expertise with the presence of state-of-the-art (bio)analytical equipment and advanced facilities that are essential pillars of robust and continuous growth. /ppTo support the growth of our Group, we are seeking new talents whose expertise will bring unique added value. /ppAt ERBC GROUP, we firmly believe that diversity and inclusion are essential to our collective success. We value differences and highlight the unique qualities of each of our team members, whether in their backgrounds, experiences, or perspectives. This commitment drives us to create a work environment where everyone feels respected, supported, and empowered to reach their full potential. /ppTrue to these principles, we place particular emphasis on integrating team members with specific needs by providing the necessary conditions to foster their growth and contributions to our shared ambitions. /ppbPosition /b /ppERBC is looking for an In Vivo Toxicology Study Director Assistant W / M to join the In Vivo Toxicology division within Pomezia Site (Rome). /pulliWHO YOU ARE /li /ulpThe Toxicology Pathology division, led by the Toxicology Pathology Sciences Director, is structured around Study Directors and Pathologists profiles. /ppThe In Vivo Toxicology Study Director Assistant W / M fulfills a range of responsibilities essential to the successful execution of research studies. As a scientific project assistant, the Study Director Assistant has the overall responsibility to support Study Directors in the conduction of non-clinical toxicology studies in rodent and non-rodent species, in compliance with National and International Regulations and with the Good Laboratory Practice (GLP). /pulliIN THIS POSITION, YOU WILL /liliSupport the Study Directors in the conduction of the studies from study design to management of the team execution of the study. /liliSupport the Study Directors to collect, analyze and interpret study data and write the scientific study reports. /liliContribute to the department scientific improvements in collaboration with his / her peers and direct managers and other internal scientific and technical staff by developing and sharing his / her own expertise. /li /ulpbProfile /b /pulliYOUR PROFILE /liliEducation / experience /liliPhD in Biological Sciences, Pharmacology, Veterinary Sciences or related disciplines. /liliExpertise in drug development strategies is a plus. /lili1-2 years of experience in managing experimental life science studies in Contract Research, Pharmaceutical, Chemical or Biotechnology Organizations is a plus. /liliWorking knowledge of AAALAC and GLP regulations and preclinical testing facility operations and procedures is a plus. /liliLanguages /liliEnglish, B2 level is required. /liliMicrosoft Office Suite /liliSoft Skills /liliExcellent organization and problem solving attitude. /liliAssertiveness proactive approach. /liliAbility to work in a team. /liliExcellent communication, interpersonal and listening skills. /liliContract : We offer a fixed term maternity replacement contract within the national collective agreement for the pharmaceutical industry. /liliTraining : People are our biggest asset, and we provide the time and budget to help you grow, through training, coaching and self-development. /liliFlexibility : We understand life is about balance and we provide flexibility and support to help you achieve your life goals, including smart working as per internal policies. /li /ul #J-18808-Ljbffr