In this role, the selected candidate will be responsible to provides input into the development of clinical monitoring plan, informed consent forms, template source documents, study manual, regulatory binder and other study-related documents as needed.
In this role, you will be responsible to recruit, educate, and obtain study subject enrollment and consent. Complete case report forms, maintain up-to-date research logs, schedule appointments, prepare recruitment patient letters, and various other study correspondence as required.
In this role, you will be responsible to troubleshoots and resolves, or refers to appropriate others, problems detected in the course of work. Demographic information, limited patient health information related to job function.
In this role, you will assist with all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files.