We are looking for a talented and motivated Safety Associate to join our team. ¿Tiene su CV preparado? Si es así y confía en que este es el puesto adecuado para usted, asegúrese de enviar su solicitud lo antes posible. As a Safety Associate you will be responsible for the day-to-day implementation and monitoring safety to ensure compliance with all relevant regulations for clinical studies.
Main Responsibilities ▪ Support management of periodic reports on clinical study safety, through gathering data, analyzing safety signals, and timely submission to Regulatory Bodies and Independent Ethics Committees. ▪ Support the implementation of safety monitoring strategies by tracking adverse events, assisting in the evaluation of safety data, and contributing to the management of reportable incidents in accordance with regulatory requirements. ▪ Verify the adequacy of the safety reports fulfilled by the clinical sties to meet pertinent regulatory and safety standards, and to be consistent with the safety databases Skills, Experiences and qualifications required ▪ BS/MS degree or similar in human health related discipline ▪ At least 1 year of experience in a safety role within biotechnology or pharmaceutical industry or other equivalent experience. xbhjioe ▪ Excellent written and verbal communication skills in English. ▪ Work effectively and productively ▪ Strong interpersonal, communication and presentation skills ▪ Very high sense of integrity and confidentiality Working conditions ▪ Full time position ▪ Offices located in the center of Barcelona ▪ Working remotely is an option ▪ Competitive Salary