Research Technology Specialist CRI Edgewood

Job Description

The Coordinator Computer Applications CRI is primarily responsible for support of the Clinical Research Institute’s use of research technology, including but not limited to REDCap, High Enroll, SharePoint, CTMS, electronic IRB, and eRegulatory system (examples: AxiomMentor, SignalPath, and Complion). The individual will provide application support to Clinical Research Institute (CRI) staff, St. Elizabeth end-users, and CRI affiliates managing requests appropriately and in a timely and professional manner. The incumbent will collaborate with system and technology administrators across Information Technology division.

Demonstrate respect, dignity, kindness and empathy in each encounter with all patients, families, visitors and other employees regardless of cultural background.

Responsibilities

• Collaborate with CRI staff and the Research IT Working Group to support CRI technology initiatives, process improvements, education, and communication efforts.
• Assist in testing and validation of research applications during application upgrades and during implementation of new functionality to ensure proper operation and freedom from defects.
• Manage access for new users.
• Serve as the liaison between CRI, IT, and end-users to assure cohesive approach to research technology use. Work with Education Specialist to ensure appropriate and timely training for end users.
• Analyze release notes for application updates and carry out procedures to ensure that all systems, products, and services meet organization standards and end-user requirements.
• Develop and maintain standard operating procedures (SOPs) and workflows that govern the use of research technology.
• Ensure the integrity and quality of data entry into research technology systems and identify and implement process improvements to enhance functionality and use.
• Perform other duties as assigned.

Qualifications

Education, Credentials, Licenses:

Bachelor's Degree in related field

Specialized Knowledge:

• Prior use of a Clinical Trial Management System (CTMS)
• (Preferred) Knowledge of EPIC, REDCap, electronic IRB, eRegulatory, and SignalPath.

Kind and Length of Experience:

Two years Clinical Research Experience

If, for any reason, you are having difficulties applying, please contact our recruitment team at recruiting@stelizabeth.com