Clinical research data coordinator - united states, pasadena (california)

adecco medical and science is looking for a skilled clinical reasearch data coordinator for west hollywood ,ca location.

job title:

clinical research data coordinator

job type - temp to hire 

time - monday to friday ( 8am to 4.30 pm )

description:

the incumbent is responsible for the data management of all clinical research studies. this includes the maintenance of regulatory files to fulfill research requirements. work with study monitor to ensure proper data collection and assist investigator and study coordinator in clinic settings.

responsibilities:

data management for all clinical research studies. this includes responsibility for collection and transcription of research patient data and study related information into research records (crfs), and maintenance of source files to fulfill research requirements

work with study coordinator to maintain screening and enrollment logs and track progress of patients on study while monitoring protocol compliance of specific study requirements

preparation for study initiation and submission of required regulatory documents such as cv’s, laboratory certificates, fda forms, 1572’s, financial disclosure forms, training certificates, delegation of authority forms, irb submission and approvals, and other miscellaneous paperwork required for study compliance to study sponsor for each research protocol

tracking and maintaining the study budget and payments, including invoicing the sponsor for completed work

provide general administrative support to the research team as needed.

operate personal computer to access e-mail, calendars, and other office software

other miscellaneous job duties that may arise in the role

 

 requirements:

bachelor’s degree in health-related field

demonstrated organizational skills to efficiently and effectively provide data management/monitoring support for multiple clinical trials and projects, providing accurate information in a timely manner.

demonstrated working knowledge of current medical terminology specific to oncology, to accurately read entries in patient charts and record accurately and timely, information into study records and other appropriate research data forms.

demonstrated understanding of confidential information, how it is defined, and demonstrated skill in maintaining confidential status of such information.  knowledge of electronic data capture (edc) database programs is a plus.

interested candidates please apply below !

equal opportunity employer/veterans/disabled



the company will consider qualified applicants with arrest and conviction records

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