Safety Expert for Clinical Trials

Há 4 dias


São Paulo, São Paulo, Brasil beBeePharmacovigilance Tempo inteiro R$104.000 - R$176.000

Pharmacovigilance Team Lead

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We are seeking a skilled and experienced Pharmacovigilance Team Lead to oversee the collection, evaluation, and reporting of adverse events. This role involves managing a dedicated team, ensuring compliance with regulatory requirements, and fostering a culture of safety and quality within the organization.

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The ideal candidate will have a strong understanding of pharmacovigilance regulations and safety reporting standards, as well as excellent leadership and organizational skills. They will be responsible for developing and implementing pharmacovigilance processes and policies, collaborating with clinical, regulatory, and quality assurance teams, and providing training and guidance to team members and stakeholders.

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In this role, you will have the opportunity to make a significant impact on the safety and efficacy of clinical trial products throughout their lifecycle. You will work closely with cross-functional teams to ensure comprehensive safety assessments and timely reporting of safety data.

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We offer a competitive salary, various annual leave entitlements, health insurance offerings, retirement planning opportunities, and a range of other benefits designed to support your well-being and work-life balance.

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If you are a motivated and detail-oriented individual with experience in pharmacovigilance or drug safety management, we encourage you to apply for this exciting opportunity.

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