Clinical Research Data Coordinator

Mayo Clinic•Phoenix, AZ

1d•Hybrid

About The Position

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.

Requirements

Must be located within 100 miles of the Phoenix campus.
Training will be on-site for five weeks.
On-site expectations of two days per month once training is complete.
Mayo Clinic DOES NOT participate in the F-1 STEM OPT extension program.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status or disability status.

Responsibilities

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.
Provides data management support for minimal risk, extramural funded, registry/database clinical trials.
Responsible as directed for data collection in a timely manner, utilizing case report forms, patient interviews, and source documentation.
Develops and designs clinical reports and creates 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.