Overview

Reference Number: JO-2005-450305
Senior Regulatory Operations Associate
Rate: Negotiable
Job Type: Contract
Location: United States

Senior Regulatory Operations Associate

Based in California

Competitive Rate of Pay

We are looking for Regulatory Operations individuals who are interested in working with a global pharmaceutical company, with a focus on EU and ROW submissions. This exciting opportunity will allow you to gain experience in global markets and be part of a global and expanding company, with an impressive pipeline.

Day to day responsibilities include:
European and Swiss eCTD Submission Publishing
ROW Publishing
Document Processing
Department Administration
Contribution towards Process Initiatives

Required experience/skills:
Basic understanding of medical/scientific terminology
Excellent level of written and verbal English
Good level of computer literacy with Microsoft applications
Very high level of accuracy and attention to detail
Excellent organization skills and ability to prioritize
Experience in European (Centralised) and Swiss eCTD, or ROW publishing or Document Processing or general administration, depending on the role

If this position is of interest to yourself, you can send your CV to ben.loader@regulatoryprofessionals.com

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