Mundipharma
Regulatory Affairs Systems and Data Manager
GB Cambridge
Sponsorship not specifiedDetected 30 days ago
Data AnalysisFDA RegulatoryCommunicationRegulatory Affairs
About the role
- Role and Responsibilities The Manager will be accountable for the strategy and management of all systems and data within the regulatory affairs function.
- You will also be responsible for regulatory data management and also management of training and SOPs for regulatory.
- Working in a highly collaborative environment this role will engage with multiple areas of the business.
Requirements
- Proven experience working in the pharmaceutical industry in a regulatory/regulatory operations function.
- Proficiency in using Veeva Vault RIM and experience in driving its implementation and enhancement
- Ability to work in a fast-paced, dynamic environment.
Benefits
- We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees.
Company info
- Join us and make a difference when it matters most!
- At Mundipharma, we are proud of the work we do to bring innovative treatments to patients.
Equal opportunity
- Building an inclusive environment where people can thrive, grow and achieve their full potential is a priority.
- We believe this isn't just the right thing, but also the smart thing to do.
- We are on a journey and will seek to move forward together through education and awareness to build a culture that welcomes and celebrates diversity and uniqueness.
- We will create a workplace environment where everyone can, every day, bring their authentic selves and is treated with dignity and respect.
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This listing is sourced directly from Mundipharma's careers page and normalized into a canonical job model.