Sameemuddin Syed
Lead Technologist @ Booz Allen Hamilton | M.D. | Informaticist | Regulatory Affairs | Drug Safety and Pharmacovigilance | Clinical Research | Project Management | Scientific / Medical Writing
- Role
- Lead Technologist at Booz Allen Hamilton
- Location
- Atlanta, GA, US
- LinkedIn followers
- 500 followers
About Sameemuddin Syed
I am a dedicated physician with extensive experience at the intersection of drug safety…
Experience
Lead Technologist
May 2024 — Present · Atlanta, GA, US
EMR Optimization and Clinical Workflow Design: Designed and managed enhancements within Cerner EMR (Power Plans, Orders, and Documentation), improving clinical workflows and reducing documentation errors by 15%, which directly supported accurate adverse event reporting and patient safety monitoring.Data Governance and Regulatory Compliance: Implemented data governance frameworks that improved data integrity and compliance by ensuring alignment with global regulatory standards and supporting clinical data quality.Healthcare Data Interoperability and System Integration: Leveraged expertise in HL7 standards and healthcare data interoperability to optimize system integrations, reducing data processing times by 10% and enabling seamless data flow for clinical decision-making and adverse event reporting.Metadata Management and Data Traceability: Developed and maintained metadata cataloging systems, enhancing traceability and auditability of clinical and safety data, which improved data retrieval efficiency and supported compliance with pharmacovigilance and clinical trial requirements.Technical Troubleshooting and System Support: Provided expert technical support for critical healthcare applications, resolving complex system issues and reducing system downtime by ensuring uninterrupted data collection/reporting for operations.Stakeholder Collaboration and Process Improvement: Collaborated with cross-functional stakeholders to design and implement system improvements, enhancing patient safety monitoring and clinician efficiency while ensuring compliance with global pharmacovigilance and clinical research standards.Risk Management and Adverse Event Monitoring: Monitored and analyzed system data to identify risks and AEs, contributing to proactive risk management strategies/supporting the company’s commitment to patient safety and regulatory compliance.
Education
Rajiv Gandhi University of Health Sciences
Bachelor's degree, Medicine
2001 — 2008
Walden University
Masters of Science in Health Informatics
2017 — 2019
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