Regulatory Affairs Manager
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Zest Scientific has been instructed to recruit an enthusiastic Regulatory professional for a leading drug development organisation in the UK. The Regulatory Affairs Manager is pivotal to the success of the organisation - you will drive continuous quality improvement initiatives relating to regulatory submissions, Ethics, and ARSAC submission processes and act as point of contact for Regulatory Authorities.
This role can be remote based in the UK, with occasional visits to the office.
- Degree educated
- Previous experience in a similar role for a pharmaceutical company or CRO
- Excellent communication skills
- Project leadership
- Ultimately responsible for leading and coordinating regulatory submissions (CTA applications, ARSAC applications and Research Ethics Committee (REC) submissions) as part of a wider project team
- As a Regulatory Affairs Manager, you will also be responsible for the authoring and review of clinical documentation prepared for submission, and will compile and submit applications and perform maintenance activities throughout the lifecycle of a clinical study
Our client is a rapidly expanding organisation at the forefront of expert research. They are actively looking to recruit a forward thinking Regulatory Affairs Manager looking to develop their career with a progressive organisation.
Our client is committed to securing the services of the right candidate and is flexible with regards to the remuneration package available. Zest Scientific is working to a strict deadline so in order to be considered for this opportunity please apply now and your application will be reviewed immediately.