I have an exciting opportunity with one of the leading Blue-Chip Pharmaceutical companies. My client is looking for a Regulatory Submissions Coordinator to join their team in preparation for the Brexit campaign.
You will be working with the archival documentation and reviewing past dossiers to get them up to date. You will be working closely with Regulatory Affairs team and the Publishing team. The ideal candidate will know the difference between CMC and Clinical dossiers and will be able to communicate effectively within a team as well as being a strong independent worker.
Other responsibilities include:
- Ensure that all registration samples and certificates required for EIRA are provided in a timely manner
- Liaise with key suppliers for the supply of samples including 3rd party contractors
- Develop relationships with internal and external customers
This role is based on a 3 month contract, however depending on the scope of the project it may be extended for a further 3 months.
Please apply ASAP for immediate consideration.