Join Our Mission to Improve Lives Worldwide The Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization and commercialization phases, in compliance with the applicable legislation.The Impact You'll Make - Collaborate in the establishment of a Pharmacovigilance network of BIAL in all countries where the company operates and in the exchange of drug safety information with affiliated companies, service providers, distributors and partners; - Contribute towards the safety information management systems and to the monitoring of defined plans ; - Collaborate on the evaluation of product safety (e.G., PSURs - Periodic Safety Update Reports); - Support the assessment of quality defects and quality issues with the potential safety impact; - Collaborate in the training on the Pharmacovigilance procedures of the BIAL; - Contribute towards the management of the system that ensures that all suspected adverse reactions reported to BIAL are collected and assessed so that they are available in at least one point in the European Union; - Understand the safetyprofiles and concerns regarding BIAL medicinal products; - Collaborate to ensurea prompt and comprehensive response to any request for information performed by the authorities regarding necessary information for the benefit-risk assessment of BIAL medicinal products; - Contribute towards quality management system regarding Good Pharmacovigilance Practices that includes quality assurance and quality control procedures, compliance monitoring, SOPs, training and audits; - Comply with Good Pharmacovigilance Practices and Good Clinical and/or Laboratory Practices, as applicable; - Comply with the Policies, Standards and Procedures in place; - Collaborate effectively with other departments, teams and colleagues as required, to support overall company objectives. What You'll Bring - Degree in Pharmaceutical Sciences or similar areas; - 0-1 years of experience in pharmaceutical industry; - Good IT skills;- Good planning and organization skills; - Assertiveness and goodcommunication and interpersonal skills; - Knowledge of Good Pharmacovigilance Practices and Good Clinical Practices (preferred); - Knowledge of epidemiology and biostatistics (preferred). Create Your "I work together with people from various backgrounds, with different expertise and beautifully complex personalities – and I love that!" Carmen Denecke Muhr (Global Medical Affairs Manager – Parkinson's, Germany) #J-18808-Ljbffr
