Regulatory Affairs
Jobs with Aerotek
Aerotek can help you find the
Regulatory Affairs job you're looking for.
Regulatory Affairs job duties may include: performing project management activities associated with the compilation of client submissions to regulatory authorities, including paper and electronic formats; reviewing clinical documentation, such as clinical study reports, protocols, and informed consents; providing regulatory guidance, training and support to staff, project teams and external clients and developing and maintaining documented regulatory procedures as required to assure consistent and compliant regulatory activities.
View all of our available regulatory affairs jobs.
-
Sr Quality Analyst
-
Scientific
-
Los Angeles, CA
-
Wednesday, May 16, 2012
-
Regulatory Affairs Manager III
-
Clinical
-
Somerville, NJ
-
Tuesday, May 15, 2012
-
Med Device Regulatory Specialist
-
Scientific
-
Monrovia, CA
-
Monday, May 14, 2012
-
SAS Programmer
-
Scientific
-
South San Francisco, CA
-
Monday, May 14, 2012
-
Sr. Regulatory Affairs Specialist
-
Scientific
-
Los Angeles, CA
-
Friday, May 11, 2012
-
Director of Medical Affairs
-
Scientific
-
Princeton, NJ
-
Friday, May 11, 2012
-
Clinical Research Opportunities
-
Clinical
-
South San Francisco, CA
-
Thursday, May 10, 2012
-
DEA Analyst
-
Scientific
-
Sunrise, FL
-
Thursday, May 10, 2012
-
Clinical Research Opportunities
-
Clinical
-
South San Francisco, CA
-
Thursday, May 03, 2012
If you do not see a/an
regulatory affairs
job that matches your skills, create
an account so we can contact you when new
regulatory affairs
jobs become available.
You can also begin a custom job
search to see similar types of jobs we have available or contact your local
Aerotek office to speak with a recruiter.