Regulatory Affais Manager

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Amar Annamalai
Amar Annamalai's picture
Regulatory Affais Manager

Global pharmaceutical company is not looking or experienced consultant to manage regulatory affairs submission for product in development stage in area of oncology.

An ideal candidate will have already gained experience in:

Clinical Trial Application to European Health Authorities
Compiling the dossier, review relevant documents and proposing strategic solution to effective strategies to file the dossier
Experience in MAA (MRP, CP, DCP) is highly desirable

Please send your CV to eval(unescape('%64%6f%63%75%6d%65%6e%74%2e%77%72%69%74%65%28%27%3c%61%20%68%72%65%66%3d%22%6d%61%69%6c%74%6f%3a%62%65%61%74%61%2e%6b%6c%65%63%7a%40%73%65%63%70%68%61%72%6d%61%2e%63%6f%6d%22%3e%62%65%61%74%61%2e%6b%6c%65%63%7a%40%73%65%63%70%68%61%72%6d%61%2e%63%6f%6d%3c%2f%61%3e%27%29%3b')) for review or call on 0207 255 6665.

Deadline: 6 December 2013

For more details