Regulatory Affairs Manager, EU, Oncology
Contract Job, Hybrid Your new company This global biopharmaceutical company is looking for an experienced Regulatory Affairs professional to join them on a contract basis. A 12-month, hybrid contract job with scope for extension. Your new role As Regulatory Affairs Manager, you will work closely with the EU Regulatory Lead within the oncology team, managing the operational and procedural aspects and providing support for new Marketing Authorisation Applications’ preparation and filings as well as Life Cycle Management for the European Centralised Procedures. In this role, you will plan and track activities related to regulatory submissions in the EU, communicate regulatory submission dates, regulatory status, nature of changes, and track and inform relevant parties of minor/significant product information changes. What you'll need to succeed Previous experience working in Regulatory Affairs and a strong working knowledge of EU regulations are essential. All applicants must have worked directly with EMEA on different types of submissions and have clinical experience. What you'll get in return Flexible working options, a good hourly rate, and a discretionary bonus. What you need to do now For more information on this or any other contract jobs in Regulatory Affairs, please apply to this job advert.
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Contract Job, Hybrid Your new company This global biopharmaceutical company is looking for an experienced Regulatory Affairs professional to join them on a contract basis. A 12-month, hybrid contract job with scope for extension. Your new role As Regulatory Affairs Manager, you will work closely with the EU Regulatory Lead within the oncology team, managing the operational and procedural aspects and providing support for new Marketing Authorisation Applications’ preparation and filings as well as Life Cycle Management for the European Centralised Procedures. In this role, you will plan and track activities related to regulatory submissions in the EU, communicate regulatory submission dates, regulatory status, nature of changes, and track and inform relevant parties of minor/significant product information changes. What you'll need to succeed Previous experience working in Regulatory Affairs and a strong working knowledge of EU regulations are essential. All applicants must have worked directly with EMEA on different types of submissions and have clinical experience. What you'll get in return Flexible working options, a good hourly rate, and a discretionary bonus. What you need to do now For more information on this or any other contract jobs in Regulatory Affairs, please apply to this job advert.
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