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Advarra has as its core function the institutional review board review (IRB) review of any and all research from survey research to first-in-human research sponsored by pharmaceutical companies, biotech companies, institutions, hospitals as well as clinics and private physician offices. The regulatory group is responsible for the expedited review of research, the full board review of research (an average of 17 weekly meetings) and the drafting and writing of the meeting meetings. The regulatory group also collaborates with other parts of the organization on thought leadership, client guidance and operational efficiencies. This position provides administrative and regulatory support to the Boards focused on scheduling meetings and Member Administration. This position will also offer general administrative support to the Regulatory Support Team and the Regulatory Department and back up coverage for the Board Member Administration Senior Coordinator.