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| Job Location | Uxbridge |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract, full-time |
CK Group are recruiting for a Regulatory Affairs Senior Manager to join a biopharmaceutical company at their site based in Uxbridge on a on a contract basis for 12 months.Company:Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics.Location: This Regulatory Affairs Senior Manager role will be based at our clients site in Uxbridge, Greater London. Salary:£49.15 per hour PAYE.Regulatory Affairs Senior Manager Role:- Ensure that the business acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as well as to market approved medicinal products.- Ensure timely regulatory compliance with above approvals, as requested this role may provide management and leadership by supervising one or more other regional regulatory leads and/or support staff (dependent on grade).- Advising on regional considerations in developing strategy.- Ensuring the regional needs are well defined and implemented in collaboration with relevant regional stakeholders.Your Background:- Regulatory knowledge in regional legislation.- Working with policies, procedures and SOPs Experience with national legislation and regulations relating to medicinal products.- Understanding of the regional regulatory procedures for CTAs, MAs, post approval changes, extensions and renewals.- Understanding of drug development.Apply:For more information or to apply for this Regulatory Affairs Senior Manager position, please contact Julie Marshall on or email , quoting job ref 48392.It is essential that applicants hold entitlement to work in the UK.