Description Clinical Trials Associate I, Hematology Oncology JOB SUMMARY: Perform a variety of duties involved in the collection, processing, interpretation, storage and documentation of biological and data specimens in support of clinical trials and database creation. Assists in ensuring adherence to protocols, appropriate regulations, and deadlines. Ensures quality of information received. KEY RESPONSIBILITIES: Assists nurse in assessing patient eligibility for approved study. Knowledgeable of protocols in order to determine specific criteria for eligibility or exclusion. Gathers complete medical history of patient. Ensures patient consent forms are c
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