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| Job Location | Cambridge |
| Education | Not Mentioned |
| Salary | £350.00 - £400.00 per day |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract, full-time |
*Pharmacovigilance Processes Manager - Global BioPharma - 12-month contract * My client is a Global Biopharmaceutical company and they have a position available for a Pharmacovigilance Processes Manager for an initial 12- month contract. Within this role the Pharmacovigilance (PV) Processes Manager will work alongside the PV Processes Leads and Principals, supporting tasks related to management of projects, processes including implementation, communication, quality, compliance, tracking, performance and inspection readiness. Accountable to develop relationships across Patient Safety and other relevant areas of the company to execute the delivery of the assigned tasks in relation to processes strategy, priorities, alongside governance and management of the current procedural documents. Main Responsibilities: * Collaborate with PV Process Leads and Principals with supporting the enhancement of existing processes * Working with the Process leads and Principals, and Patient Safety (PS) and Regulatory experts, develop, establish, monitor, report and assess global KPIs related to safety and regulatory data reporting. * Support PS Process owners with guidance, advice and support on Process Development process. * Author and collaborate with SMEs to deliver assigned Toolkit documents and templates. * Maintain and continuously improve key customer facing service solutions for Process guidance and document access (R&D Process Portal, Lollipop, PSDM SPOL, Q&A ticket portal etc). * Coordinate specific tasks related to procedural document management to provide oversight to the Pharmacovigilance (and PS) process teamIn order to apply for the Pharmacovigilance Processes Manager contract, you should possess a Life Sciences degree, project management experience, knowledge of Patient Safety operating model and organisation. You must have experience of working in a global organisation within the Pharmaceuticals industry and have experience of the drug development cycle and commercial aspects of the industry. Experience of working with Procedural documents is a must as are administrative skills including SharePoint. Before you apply for this position it is vital that you are in possession of an EU or UK passport or relevant visa to work without restrictions in the UK. To apply for this position or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on . Required skills
Keyskills :
Patient Safety Pharmaceutical Pharmacovigilance SharePoint PV Contract Project management Pharma PV Processes procedural documents