As a key member of the Hematology clinical research team, you will be working with a team of 20+ clinical researchers to find better treatment options for the hematology patient population. This job entails coordination of clinical trials from start to finish and regulatory experience is preferred. Studies in this group could be therapeutic or non-therapeutic and deal with sick cell hemophilia, or other hematologic disorders.
Your primary responsibilities will revolve around creating protocol documents, consenting patients, abstracting data from medical records, completing case report forms and entering data. You will maintain regulatory compliance by submitting applications for review and approval by the St. Jude regulatory committees. You will act as a liaison among key stakeholders in the institution and facilitate study team meetings. Study deadlines need to be met while navigating the logistics of scheduling around patient visits. Take the first step to join our team by applying now.
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