Requires the Specialist to have at least one year of clinical research experience to ensure adequate knowledge of research and institutional systems to decrease the length of onsite training and increase project productivity.
June 19, 2020
Assist the disease team in developing strategies to ensure increased study awareness, subject enrollment, protocol compliance, including maintenance of protocol information tools for assigned disease team.
June 28, 2020
Develops and maintains regulatory and legal documents per guidelines and regulations of the research/study sponsor and the participating institution per IRB, FDA, PHA and other applicable regulatory agencies.
August 03, 2020
Maintains screening, enrollment, adverse event, deviation, tumor measurement, concomitant medication, delegation and other sponsor and/or protocol specific logs.
August 11, 2020
Reviewing for potential subjects and handle referrals as they are forwarded to the sites and triaging participants into the appropriate studies.
September 18, 2020
Demonstrated working knowledge of current medical terminology specific to oncology, to accurately read and comprehend patient study information and record accurately and timely, information into study records and other appropriate research data forms.
September 26, 2020
Performs accurate data collection and reporting according to protocol requirements and completes applicable forms and/or other required reports in a timely manner.
September 28, 2020