Description
Our client a large pharmaceutical company require an experienced Regulatory Affairs Consultant to prepare and submit and follow up registration applications to UK and European regulatory authorities and assist and provide support in the preparation, distribution and follow up of registration documentation to affiliate organisations in other European countries as required.
This is a consultant role working on various projects. The role will include the management of marketing authorisation applications, prepare and submit the necessary documentation to regulatory authorities, developing a comprehensive understanding of the regulatory requirements.
Skills Required:
Degree or High Level Qualification in Life Science, Proven experience with Pharmaceutical Research and Development process, Strong Written and Oral Communication skills, In depth experience of Regulatory Requirements within the Pharmaceutical Industry.