There’s a reason St. Jude Children’s Research Hospital is consistently ranked on Fortune Magazine’s “100 Best Places to Work For” list. At our world-class pediatric research hospital, every one of our professionals shares our commitment to make a difference in the lives of the children we serve. In the role of Clinical Research Regulatory Affairs Associate, you will be responsible for assisting in the coordination of clinical research components as they relate to investigational products under the purview of the Food and Drug Administration (FDA), Recombinant Advisory DNA Committee (RAC) and Office of Biotechnology Activities (OBA).
We are an “all-in” type of culture and you play a key role in keeping our standards high for clinical research activities. This type of work involves you gaining rapport and credibility with internal and external stakeholders. Responsibilities include assisting study teams with creation and approval of drug/biologic/device applications, developing regulatory documents, and representing St. Jude as a point of contact to the external regulatory authorities. You will have the opportunity to be on the cutting edge with experimental studies with direct principal investigator interaction. Take the first step to join our team by applying now!
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