Sr Associate Regulatory Affairs

Location: Thousand Oaks, CA
Date Posted: 06-12-2017
Day to Day Responsibilities:
Able to work independently and to assist projects as appropriate.

Responsible for supporting the Global Labeling Strategists for assigned products and adminstrative tasks relating to process and procedures. Has knowledge of commonly-used concepts, practices, and procedures within a particular field. Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision. Typically reports to a supervisor or manager.

Ideal candidate - Previous Amgen experience is preferred, Industry experience in Regulatory, Labeling, or Clinical space. Technical skills are a must for this role i.e, EPIC and MS office and Documentum experience, Experience in competitor searches using Cortellis, Doctor Evidence, etc. (These are software tools used to search for competitor labeling, regulatory intelligence. Minimum of 1-2 years industry experience in the clinical or biological space.

Experience in a regulated industry, science academia or clinical practice

"This posting is for Contingent Worker, not an FTE"
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