Descripción de la oferta
Overview
We are looking for a talented and motivated Safety Associate to join our team.
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.
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 sites to meet pertinent regulatory and safety standards, and to be consistent with the safety databases.
Qualifications
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.
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
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