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The role involves managing Individual Case Safety Reports (ICSRs), providing support in activities related to pharmacovigilance, ensuring effective cooperation with clients, and performing various administrative and reporting tasks within the ICSR management unit under supervision.
The Senior Safety Technology Support Specialist is responsible for leading support related to safety databases and technological applications used in pharmacovigilance. Duties include gathering user requirements, liaising with the Safety Systems team, participating in audits and testing, and providing user training. The role also involves maintaining SOPs, assisting with regulatory needs, and mentoring junior staff while supporting the implementation of safety system enhancements and efficiencies.
The Regional People Generalist is responsible for administering HR policies and operations, supporting onboarding and offboarding, managing employee documentation, and providing HR-related advice. They will also facilitate talent management programs and ensure compliance with labor regulations while promoting a conflict-free workplace.
The PV Associate/Literature will be responsible for supporting literature monitoring, screening activities, assisting with literature search strategies, reviewing literature articles, tracking data, and ensuring compliance with regulations. The role requires strong communication, organizational skills, and attention to detail while working under supervision and assisting with the development of screening processes.
The IT Technical Support Engineer provides technical support to internal and external users, manages support tickets, performs troubleshooting, and maintains company systems including laptops and servers. They are responsible for responding to incidents, documenting resolutions, and training personnel in IT procedures.
The PV Associate/Literature assists in literature monitoring ensuring compliance with regulations, contributes to company goals, and participates in literature searches and screenings. They maintain records and track literature, assist in quality checks, and support the team in regulatory inspection preparedness.
The PV Associate role is designed for recent graduates in life sciences or healthcare fields. Responsibilities include processing safety reports, reconciling received reports, and supporting pharmacovigilance activities while working under supervision. The position emphasizes training, teamwork, and a proactive approach to patient safety.
The role involves monitoring local scientific literature and safety web portals for adverse event reports. Responsibilities include formulating search strategies, translating relevant documents, maintaining files according to procedures, and ensuring compliance with data privacy and security standards.
The role involves performing local scientific literature monitoring for adverse event reports, formulating search strategies, providing translations of documentation, and ensuring compliance with data privacy and security procedures.
The PV Associate role involves processing Individual Case Safety Reports and supporting pharmacovigilance activities, ensuring compliance with regulations and high-quality data management. The position is aimed at new graduates looking to start their career in drug safety and includes mentoring from experienced colleagues.
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