Shreya Giri

• Understand the current Pennsylvania (PA) LIMS system and the State Health Laboratories' LIMS business needs to assist in the implementation of a new LIMS system that aligns with program requirements.
• Collaborate with internal and external stakeholders to ensure the new LIMS system meets operational and compliance needs.
• Partner with business stakeholders to gather, document, and analyze requirements for the new LIMS system, ensuring alignment with laboratory objectives.
• Conduct gap analysis between the current LIMS system and the proposed solution to identify business process improvements and recommend optimizations.
• Drive the identification of as-is processes across business units to define system enhancements and ensure smooth transition.
• Work closely with testing teams to provide Subject Matter Expert (SME) inputs and assist in User Acceptance Testing (UAT) to validate system functionality.
• Configure and customize LIMS modules to align with laboratory operations while ensuring regulatory compliance(GLP, HIPAA, FDA 21 CFR Part 11, ISO 17025).
• Develop Business Requirement Documents (BRD), Functional Specification Documents (FSD), User Stories, and Use Cases to define system functionalities.
• Act as a liaison between business users, technical teams, and vendors to facilitate clear communication and ensure project success.
• Conduct training sessions and create user manuals to support end-users in system adoption and operational efficiency.
• Ensure smooth data migration, integration, and reporting by coordinating with IT teams and validating data accuracy.
• Monitor system performance post-implementation, gather user feedback, and recommend continuous improvements for optimized laboratory operations.
• Understand the current Pennsylvania (PA) LIMS system and the State Health Laboratories' LIMS business needs to assist in the implementation of a new LIMS system that aligns with program requirements.
• Collaborate with internal and external stakeholders to ensure the new LIMS system meets operational and compliance needs.
• Partner with business stakeholders to gather, document, and analyze requirements for the new LIMS system, ensuring alignment with laboratory objectives.
• Conduct gap analysis between the current LIMS system and the proposed solution to identify business process improvements and recommend optimizations.
• Drive the identification of as-is processes across business units to define system enhancements and ensure smooth transition.
• Work closely with testing teams to provide Subject Matter Expert (SME) inputs and assist in User Acceptance Testing (UAT) to validate system functionality.
• Configure and customize LIMS modules to align with laboratory operations while ensuring regulatory compliance(GLP, HIPAA, FDA 21 CFR Part 11, ISO 17025).
• Develop Business Requirement Documents (BRD), Functional Specification Documents (FSD), User Stories, and Use Cases to define system functionalities.
• Act as a liaison between business users, technical teams, and vendors to facilitate clear communication and ensure project success.
• Conduct training sessions and create user manuals to support end-users in system adoption and operational efficiency.
• Ensure smooth data migration, integration, and reporting by coordinating with IT teams and validating data accuracy.
• Monitor system performance post-implementation, gather user feedback, and recommend continuous improvements for optimized laboratory operations.

TIMS Project:

• Analyze the current Illness Monitoring System (TIMS) and identify business needs to assist in its implementation, enhancement, and optimization in collaboration with internal and external stakeholders.
• Partner with public health officials, healthcare providers, and IT teams to gather, document, and analyze requirements for the new TIMS system.
• Ensure the system meets regulatory requirements such as HIPAA, CDC guidelines, and state health policies for data security and compliance.
• Develop RTM document based on needs of the stakeholders.
• Collaborated with Microsoft to identify and implement the best solution for the Illness Monitoring System (TIMS)using Power Pages and other Microsoft technologies.
• Create meeting minutes for different meetings and document all necessary documents on SharePoint.
• Worked with PM to track the provisioning of Power Apps premium and Power automate Licenses ensuring timely assignment.
• Schedule and Coordinate initial design sessions with Microsoft and internal stakeholders.

• Monitored incoming contracts and service agreements for correct pricing and information.
• Researched laws and regulations potentially impacting company policies and procedures.
• Coordinated and attended meetings representing the firm as the Point of Contact to review contractual obligations.
• Analyzed contracts for various departments using both manual and automated strategies.
• Analyzed 50-80 Contracts per day.
• Contracts focusing on Post-merger Customer Account Integration, Sales enablement and Support for Sales Operations, Legal Risk Mitigation and Financial Compliance, and Renewal Management