Regulatory Document Management Software Specialist

Regulatory Document Management Software Specialist
Warszawa
NR REF.: 1089357

Currently for our client, pharmaceutical company with an office in Warsaw, we are looking for experienced Document Management Specialist who worked with regulatory documents.

What will you be doing?

On this position you will be responsible for every aspect of managing the rDMS and serving as the first point of contact to the end users from different divisions like Clinical Trial or Regulatory Affairs. The users may require assistance regarding system access and/or some business support and you need to be ready to provide it.

Who are we looking for?

You need to be communicative, supportive and accessible person to be able to provide help successfully. You will be responsible for managing documentation associated with clinical trials but meritorious knowledge of the subject is not necessary. You need to speak English very well though because you will be working in an international environment.
Also, since the company works on self-developed eDMS, we require first-hand experience in working with any software used for this purpose (knowledge of rDMS is nice to have).

What do we offer?

In return for your knowledge and commitment the company offers very attractive salary and employment conditions (broad range of benefits, stable employment contract and many opportunities for development).

Advance your career and apply!