Description
Major pharma in northern New Jersey seeking Submissions Coordinator for 6 month contract.Job purpose:
Provides support including, but not limited to, the following for the Global Regulatory Operations team: Archiving of Health Authority correspondences, MS Word and PDF processing, and document and record management.
Responsibilities will include, but are not limited to, the following:
* Provide MS Word processing support for preparation of regulatory submission documentation.
* Responsible for the archiving of Health Authority correspondences.
* Provide Adobe PDF processing support for preparation of regulatory submissions.
* Assists the Global Regulatory Operations Publisher in regulatory document and records management.
* Assist with data entry in the Regulatory Affairs tracking system
* Provide system support to users of regulatory systems
Great company to work for, have a few contractors on site at the moment and they are very happy. Wonderful team to be a part of.
If you are interested or know anybody who might be, please send an updated CV and the best phone number to reach you on.