Drug Safety Associate II

Job title: Drug Safety Associate IILocation: Maidenhead - Hybrid (2-3 days per week in the office)Contract length: 18 month initial contractRandstad Sourceright, a leading provider of RPO & MSP Recruitment Services are currently recruiting for a Drug Safety Associate II / Pharmacovigilance Specialist on behalf of a global biotechnology company in their Safety and Benefit Risk Management (SABR) business unit. This role is an initial 18 month contract to be based in their Maidenhead offices on a hybrid basis.The Safety Associate II will be a supporting member of the Global Case Management (GCM)/International Pharmacovigilance (IPV) group who performs daily monitoring of expedited submissions and implementation of the overarching Pharmacovigilance (PV) operations as it relates to the businesses Partners, Distributors (International Partner Markets [IPM]), Vendors and the wider PV network that includes stakeholders worldwide and other functional groups including but not limited to Worldwide Medical, Commercial, Quality, Regulatory and Global Marketing.Responsibilities: * Contributes to oversight of Partners, Distributors, Vendors, including metrics, and review of IPM trackers. * Supports the Organised Data Collection Programs (ODCPs) process for AE collection to ensure consistency with regulations and with departmental goals and objectives. * Supports the collection, analysis, communication, and operational change management process for Regula...