Regulatory Affairs Project Manager

Updated: about 2 years ago
Location: Los Angeles, CALIFORNIA
Deadline: The position may have been removed or expired!

Qualifications

Required:

• Clinical research experience, with in depth knowledge of clinical oncology as it pertains to clinical trials and studies.

• Demonstrated organizational skills to efficiently and effectively provide data management/monitoring support for multiple clinical trials and projects, providing accurate information in a timely manner.

• Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc.



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