Overview

Reference Number: JO-2005-450307
Regulatory Operations Associate
Rate: Negotiable
Job Type: Contract
Location: United States

Regulatory Operations Associate
12 month interim contract
– California based
– Highly competitive salary

Clinical Professionals are currently recruiting for a Regulatory Operations Associate to join a global pharmaceutical company, with a focus on EU and ROW submissions.

This exciting opportunity will allow you to gain experience and be part of a global company who are developing a number of drug treatments across a wide range of therapy areas.

Key responsibilities shall include:
– Creating electronic navigation and publishing of submissions to the relevant Regulatory agencies
– Communicating with the Regulatory Affairs lead
– Troubleshooting issues with systems or documents
– Document formatting of Clinical Study Reports

Required qualifications and experience:
– 1-2 years relevant work experience
– Excellent written and verbal communication
– Basic understanding of medical/scientific terminology
– Good level of computer literacy
– High attention to detail and time management skills
– Experience in general administration is desirable

If this role is of interest please submit your CV to myself at: sarah.phillips@clinicalprofessionals.co.uk