Clinical Trials System Administrator

Responsible for the application support and maintenance activities of the clinical research applications utilized at CRHI and across the Network. This individual assists with training staff in the use of these systems and coordinates reporting needs.

Responsibilities:

* Perform in depth analysis of research operation workflows and data collection methods.

* Create workflow diagrams and step-by-step process documentation.

* Identify opportunities for process optimization and implement solutions.

* Participate in the integration efforts between the Network Clinical Trials Management System and other clinical operating systems (i.e. EPIC).

* Consult and collaborate with the clinical research management teams to review reporting needs.

* Prepare reports and dashboards; run ad hoc queries.

* Assist in testing and system validation.

Qualifications/Requirements:

Experience:

* Five years of experience in systems analysis and application program development.

* Proficient in Microsoft Excel.

* Knowledge of Microsoft Visio preferred.

* Knowledge of Tableau preferred.

* Knowledge of OnCore/Clinical Trials Management Systems preferred.

* Knowledge of EPIC preferred.

Education:

Bachelor's Degree or equivalent combination of education, training and/or experience that demonstrates the ability to perform the duties of the position

Licenses /

Certifications:

Other: