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Clinical Trials Associate I
Description Clinical Trials Associate I - Term JOB SUMMARY: This is a full-time, hourly term position lasting approximately 7 months. Performs a variety of duties involved in the collection, interpretation, and documentation of data in support of clinical trials. 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 completed. R


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