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Manager/Senior Manager, Pharmacovigilance

Job LocationCambridge, Cambridgeshire
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Safety Reporting Management for global leading CRO Our client is a well-established and market leading CRO based in Cambridge. They are now searching for a manager and senior manager to join the central safety reporting function and manage a team of pharmacovigilance professionals, performing oversight andcoordination of safety tasks. The team is growing due to increased demand, new clients, and product expansion. This is an exciting opportunity to work with an ever-expanding and diverse portfolio, ranging from support services relating to COVID-19 vaccinesthrough to end-to-end support for rare diseases. Your new company has a strong focus on staff development and working as a team. They are renowned for their award-winning training programmes, want to see you succeed and provide continuous support and development initiatives. As well as this, they offer agreat multi-cultural environment, continued career advancement opportunities and further benefits focused on the health and wellbeing of their employees. You will be acting on a local and global scale, managing the safety team and multiple aspects of projects, staffing, and ensuring overall compliance. There will be collaboration with the senior management team and project managers to ensure continual processimprovement, consistency, and optimal performance. This will include providing strategic direction and ensuring the company has sufficient resources, as well as planning and providing accurate forecasts for projects and ensuring timely progress. Your main responsibilities will be: - Project management- Staff management (i.e., performance management, 1-1 appraisals and meetings, mentoring, development, staffing and interviewing)- Cross-functional collaboration for process improvement and problem solving- Presenting and preparing proposals- Ensuring compliance, quality and implementing corrective/preventative actions- Reviewing PV & regulatory publications/information To be successful in this role, you should have previous dealings with the above that provides the knowledge, skills, and abilities to perform the job, as well as a strong background in management and leadership. A CRO background is preferred in a safety reportingsetting, as well as a track record of pushing through initiatives.

Keyskills :
CROoperationsmanagerseniorLife Sciencepharmaceuticalqualityquality assuranceofficerauditorpharmadrug safetypharmacovigilancebiotechassociatecase processingqudit

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