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Global Regulatory Affairs Manager: EU/UK CTA Strategy
Job summary
A leading global Regulatory Solutions provider is looking for a Regulatory Affairs Manager to support the development and execution of global regulatory strategies for investigational submissions. This remote role focuses on ensuring compliance with EU and UK Clinical Trial Regulations. Responsibilities include managing submissions, collaborating with multidisciplinary teams, and ensuring regulatory compliance. Ideal candidates will have strong attention to detail and experience with regulatory submissions. Join to work on impactful regulatory initiatives that support global transparency.
Benefits
Qualifications
- Overall knowledge of regulations supporting EU Clinical Trial Regulation and UK Medicines regulations.
- Proven ability to manage time-intensive deliverables.
- Strong attention to detail in data accuracy.
Responsibilities
- Develop global regulatory strategy and manage lifecycle regulatory activities.
- Collaborate with global regulatory team on submissions and address regulatory issues.
- Perform quality control on CTA submissions.
- Coordinate CTA activities with multidisciplinary teams.
Skills
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.