Study Coordinator
About The Position
This position is in the Division of Nephrology, with a primary assignment to the clinical studies in chronic kidney disease working with the principal investigator. Current kidney studies include studies of complications of kidney disease and improving kidney health. The Study Coordinator assists the Principal Investigator with managing the recruitment of study participants and collection of data. POSITION RESPONSIBILITIES The Study Coordinator assists the Principal Investigator with the management of the recruitment of study participants and collection of data.
Requirements
- Bachelor’s degree is required
- Speaks clearly and expresses self well in one-on-one conversations and groups
- Develops effective written communications and uses them appropriately
- Interacts and pro-actively shares information with internal and external contacts where appropriate
- Develops effective relationships with peers,and other employees
- Assumes responsibility to ensure issues/concerns will be addressed and monitors them through conclusion
- Identifies, defines and analyzes information and situations before recommending a course of action
- Effectively manages own time and resources
- Seeks to apply technology and innovation to improve efficiency and solve problems
- Outstanding judgment, initiative and attention to detail are essential.
- Must be able to manage competing priorities while supporting more than one project
Nice To Haves
- Bilingual applicants encouraged to apply
Responsibilities
- Work with Principal Investigator to refine and finalize research protocols, draft study questionnaires and data collection tools
- Assist throughout IRB approval process
- Implement study protocols
- Perform data collection and quality control of study data
- Oversee the process by which participants are recruited into the study, adherence to research protocols in obtaining informed consent,blood drawing and testing, data collection and management and participant confidentiality
- Develop and implement methods to track and follow-up with study participants
- Coordinate data safety monitoring and produce quarterly reports
- Oversee questionnaires for completeness and accuracy
- Arrange meetings of study partners, develop meeting agendas,and facilitate meeting
- Implement quality control procedures
- Assist in the preparation of grants for future studies
- Develop and manage REDCap database
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
1,001-5,000 employees
