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You will be updated with latest job alerts via emailThe Data Coordinator abstracts clinical and demographic data for all levels of management with information necessary for use in planning developing and improving clinical outcomes. Designs develops implements and maintains reports abstracted from IDX systems referring physicians and hospital systems in order to monitor outcomes for the program for research projects and for reporting to state and national organizations.
Overview for Clinical Research Data Coordinator:
The Clinical Research Data Coordinator provides data management support for minimal risk extramural funded registry/database clinical trials. The data coordinator is responsible as directed for data collection in a timely manner utilizing case report forms patient interviews and source documentation. Responsibilities include the development and design of clinical reports and creation of standard and ad hoc clinical reports as needed to support regulatory requirements and/or clinical departments. Provides clinical data support for performance measurements and continuous improvement efforts. Participates in Disease/Discipline Oriented Groups (DOGs) identifying clinical data needs. Independently prioritizes assignments and completes ongoing tasks following established Clinical Research Unit and research regulatory guidelines. Provides support for Institutional Review Board (IRB) research driven studies with extramural funding. Performs other administrative duties as directed by the Clinical Research Unit Operations Manager.
As a hybrid role this is a work arrangement that supports a combination of offsite (remote) and on-site work according to business needs. On-site expectations are determined by the supervisor and will be discussed during the interview.
During the selection process you may participate in an OnDemand (pre-recorded) interview that you can complete at your convenience. During the OnDemand interview a question will appear on your screen and you will have time to consider each question before responding. You will have the opportunity to re-record your answer to each question Mayo Clinic will only see the final recording. The complete interview will be reviewed by a Mayo Clinic staff member and you will be notified of next steps.
*Visa sponsorship is not available for this position is not eligible for F-1 OPT STEM extension.
High school diploma or GED required. Associates degree preferred.
Expertise in the use of statistical computing and data management systems.
Excellent written oral and interpersonal communication skills.
Demonstrated success in meeting deadlines working independently providing education (seminars/training) being innovative and proactive in solving problems and learning medical terminology.
Strong working knowledge of PC workstations and Microsoft applications such as Access Visio Excel and PowerPoint.
Proficiency with word processing spreadsheets and database management.
Required Experience:
IC
Full-Time