Key People Pharmaceutical: Senior Regulatory Associate

Negotiable:

Key People Pharmaceutical:
Overview:
Within this role you will be responsible for preparing and filing necessary regulatory documents for clinical trial applications and handling interactions with clinical study teams and regulatory LOCs/Hubs regarding clinical trials activities. T
South East England, England

This position, Key People Pharmaceutical: Senior Regulatory Associate, was posted on February 10, 2012. Since this job has been published, it has been viewed 23 times.