Intellectt INC
Location
Alameda, CA | United States
Job description
Role : Clinical Research Associate (CRA) - B
Location : Alameda, CA - 94502
Duration : 06 Months
Description:
Must have a minimum of 2 years experience with "clinical research monitoring". Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary. Education: Minimum Associate degree (but prefer Bachelor's) and 2 years of Monitoring experience. Challenges : Monitoring position and local to San Francisco Site. Travel - Average 20 to 35 % depends on what is going on and could be anywhere in the United States.
Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary. 3-5 Years Experience Level.
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