GENERAL ACCOUNTABILITIES
You will have responsibility for delivering the new MIS/RBAC workstream within UPMC Ireland. You will implement the programme within the project scope and governance, including identification of your stream’s stakeholders. You will establish your project team and allocate responsibilities. You will collaborate with the other clinical workstream leads where required.
For the workflows to be deployed, you will be responsible for the end-user experience, the MIS/RBAC facing modules, milestone tracking and reporting workstream status and issues, risks and benefits. You will lead the decision-making process towards the resolution of issues impacting your workstream alongside the Technical Stream Lead.
Team Leadership & Stakeholder Engagement:
- Serve as the primary liaison to the end-users ensuring system design meets clinical and business documentation and workflow needs.
- Leads MIS/RBAC engagement sessions, adoption planning, and go-live readiness efforts.
- Recommend policy changes and process improvements related to MIS/RBAC use to drive efficiencies and improve outcomes.
- Facilitate regular workgroup meetings, track milestones, document decisions, and escalate risks.
- Support development of training materials and assist with education for MIS/RBAC services and other relevant end-users.
- Provide hands-on support during go-live and stabilisation phases, ensuring continuity of operations and rapid issue resolution.
- Collaborate with the training team to ensure clinicians and other relevant users are adequately trained on MIS/RBAC workflows within Meditech and associated applications.
- Support the planning and delivery of handover training to the future EHR BAU team members.
- Collaborate with MIS/RBAC governance to support ongoing optimization and training needs.
Workflow & System Design:
- Collaborate with clinical, business and technical teams to support end-to-end integrity across modules.
- Act as the subject matter expert (SME) for MIS/RBAC-related functions in MEDITECH.
- Lead the creation of detailed role-based security templates that reflect user responsibilities, workflows, and scope of practice in MEDITECH Expanse.
- Collaborate with MEDITECH analysts and operational leaders to design and validate MIS/RBAC workflows within MEDITECH Expanse.
- Support the design and enforcement of segregation of duties, minimum necessary access, and access controls across MEDITECH modules (e.g., EMR, PCS, Sched, Lab, Pharmacy, Admin).
- Review system functionality related to MIS/RBAC functions.
- Ensure MIS/RBAC operational workflows translate effectively into clinical and business processes.
- Support the integration of MIS/RBAC workflows with financial processes to ensure access integrity and optimised workflows alongside clinical and quality compliance requirements.
- Contribute to policies, SOPs, and training resources related to user access management and system login procedures.
Implementation Support, Data Validation & Testing:
- Oversee the build and configuration of security profiles and access templates in MEDITECH, including the User Dictionary.
- Lead testing activities for MIS/RBAC, including integrated and user acceptance testing (UAT).
- Identify and troubleshoot issues in collaboration with IT, finance, and clinical teams.
- Ensure MIS/RBAC is integrated with other clinical systems (e.g., lab, imaging, pharmacy) to support seamless care delivery and documentation.
- Validate statutory, management and operational reporting requirement delivery for patient access functions.
- Conduct comprehensive user access audits and validation exercises to ensure access is accurate and compliant with internal policies and external regulations.
- Coordinate and participate in integration testing (SIT), user acceptance testing (UAT), and go-live preparation activities specific to security and access control.
- Provide frontline support for troubleshooting access issues, including user provisioning, account lockouts, and permission conflicts during and post go-live.
- Champion change management among staff, addressing workflow impacts, practice changes, and documentation requirements.
- Facilitate standards development processes and actively engage MIS/RBAC SMEs in design and optimization discussions.
- Support the identification of appropriate hardware solutions for MIS module end-users in their operational settings.
Documentation & Governance:
- Maintain accurate and up-to-date project documentation, including current state/future state maps, risk/issue logs, decision registers, benefits registers, and change logs.
- Support governance processes by preparing materials for the Technical Design Forum and senior management meetings.
- Define and track key performance indicators (KPIs) readiness, adoption, and post-go-live performance.
- Assist in documenting lessons learned and continuous improvement initiatives.
- Ensure compliance with statutory and regulatory requirements related to clinical safety and digital health.
Qualifications & Experience: