Sr. Research Program Coordinator
Company Name:-
Johns Hopkins University
Job Location:-
Baltimore, MD 21287 (Orangeville area)
Job Summary:-
Job detailsSalary$38,920 – $53,520 a yearJob TypeFull-timeFull Job DescriptionGeneral Summary/Purpose:
Under the direct supervision of the Clinical Research Program Manager or the Principal Investigator, the Sr.
Research Program Coordinator is responsible for monitoring the clinical course and collection of research data on patients entered onto research protocols at the Sidney Kimmel Comprehensive Cancer Center and participating sites.
The Sr.
Research Program Coordinator is responsible for the organization, entry, maintenance and accuracy of all clinical research data for complex and detailed clinical trials, and may assist with orientation of less senior research staff in protocol and clinical research information.
This is an intermediate level position in managing clinical trials and/or registry databases within the research program.
Specific Duties and Responsibilities:
Maintains good working knowledge of all assigned protocols and reporting requirements.
Works on complex clinical studies which require a high level of knowledge, coordination, and data abstraction.
Transmits and distributes protocol information.
Responsible for submission, verification, and maintenance of protocol specific information on the SKCCC Research Protocol Library.
Maintains regulatory binder for each assigned protocol.
Prepares and submits annual renewal requests, amendments, and adverse event reports with clinical input according to IRB and Sponsor requirements.
Adheres to all protocol requirements to ensure the validity of the clinical research data.
May assist the principal investigator and/or program manager in defining information and plans required to accomplish goals of studies.
Will design and create protocol specific case report forms as needed.
May also assist less experienced staff in design and creation of such forms.
Verifies patient eligibility for studies by comparing patient history and clinical laboratory results with protocol requirements.
Confirms patient registrations and relevant data points in databases for the SKCCC Clinical Research Office and Oncology Information Systems.
Maintains a research chart for each patient.
Collects, enters and compiles clinical data from a variety of sources.
Ensures accuracy and
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