Regulatory Affairs Project Manager

Regulatory Affairs Project Manager-Pharma

Regulatory Affairs Project Manager-Pharmaceuticals

#12268 - On site Project Manager. Experience in pharmaceutical or scientific regulatory environment. Must have worked with clinical processes, drug development, FDA document submission processes or related FDA oriented regulatory processes.

Manage multiple projects at various levels, both personnel and tasks/processes. Must have experience in one or all of above in order to step in where needed. Global pharma regulatory processes, so experience in global setting preferred. Familiarity with FDA, GMP, compliance standards and document control processes and software necessary.

Position is a high-profile role but part of a larger team. Ability to work in a fast-paced team setting, flexible, willing to step in where needed, tremendous detail skills and organizational abilities. Bachelors requires, Masters highly preferred. Scientific degree required. Certification not necessary but preferred and knowledge of Six Sigma desired, but not a deal breaker.

Keys: Bachelors degree, science degree, drug development, clinical knowledge in pharmaceutical industry, regulatory affairs, document control, FDA, GMP.

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http://jobview.monster.com/Regulatory-Affairs-Project-Manager-Pharma-Job-Lake-Bluff-IL-US-83367504.aspx

This position, Regulatory Affairs Project Manager, was posted on September 15, 2009. Since this job has been published, it has been viewed 202 times.