Regulatory Intelligence Expert
6 hours ago
Randstad Sourceright is a leading provider of RPO & MSP Recruitment Services. We 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 based in Maidenhead offices on a hybrid basis. The successful candidate will have experience of working in the Pharmaceutical Industry and knowledge of good GVP practices.
In this role, you will be responsible for contributing to the oversight of Partners, Distributors, and Vendors, including metrics and review of IPM trackers. You will also support the Organised Data Collection Programs (ODCPs) process for AE collection to ensure consistency with regulations and departmental goals.
The ideal candidate will have a degree in a Science or Healthcare related area and excellent written and verbal communication skills. You will also have proficiency in Microsoft Office suite, particularly MS Excel and Sharepoint.
This is an exciting opportunity to work on drug safety activities and processes in a dynamic environment. If you are a motivated and self-starter individual looking for a new challenge, please apply today
Key Responsibilities- Oversight of Partners, Distributors, and Vendors
- Contribution to ODCPs process for AE collection
- Support to IPM leadership in development and management of technology solutions
- Experience of working in the Pharmaceutical Industry
- Knowledge of good GVP practices
- Degree in a Science or Healthcare related area
- Excellent written and verbal communication skills
- Proficiency in Microsoft Office suite
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