Pharmatek

• Lead the harmonization of workflows and test methods • Develop comprehensive Business Requirement Documents (BRD), User Stories, and Use Cases • Serve as a liaison between business units and technical teams • Create detailed functional designs, including workflows, data models, and integration plans

• Spearhead design, implementation, and optimization of Clinical LIMS solutions • Drive technical strategy and oversee entire development lifecycle • Ensure seamless integration, data integrity, and system efficiency across laboratory operations

• Author and maintain CSV documents for the mAlert program. • Build and implement program governance around CSV document approvals. • Drive document approvals with relevant stakeholders. • Troubleshoot and configure integrations between ODH, DeltaV, Syncade, and other systems that provide data to the mAlert platform. • Ensure data accuracy and integrity within all CSV files. • Collaborate with team members and stakeholders to gather necessary data and information for CSV documentation. • Adhere to company standards and protocols for data management, documentation, and system integration. • Provide regular updates and reports on the status of CSV documentation tasks and system integrations.