About
Highly accomplished Health Informatics professional with a PharmD and Master's in Health Informatics, bringing 6+ years of hands-on experience in clinical data management, data quality assurance, and regulatory compliance. Expertly integrates clinical knowledge with advanced data management and analytics tools to optimize healthcare delivery, enhance patient outcomes, and drive data-driven decision-making. Proven ability to lead clinical data strategies, manage data flow, ensure data quality and integrity, and implement robust data solutions in compliance with regulatory standards, aligning perfectly with the Clinical Data Manager role at Duke University School of Medicine.
Work
IU School of Medicine
|Research Data Analyst
Indianapolis, IN, US
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Summary
Led complex data analysis for behavioral and neuroimaging studies, collaborating with interdisciplinary research teams to advance psychiatric and neuroscience research outcomes.
Highlights
Analyzed large behavioral and neuroimaging datasets using specialized tools (Lafayette Instruments ABETII, Inscopix in vivo calcium imaging) to extract critical insights, supporting advanced psychiatric and neuroscience research.
Provided expert assistance in in vivo electrophysiology data analysis, troubleshooting Ethovision-Matlab integration to ensure seamless data processing and integrity.
Collaborated with diverse interdisciplinary research teams to design robust data collection strategies and interpret findings, directly advancing psychiatric and neuroscience research initiatives.
GTechnologies Pty Ltd
|Data Analyst Intern
Remote, Remote, US
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Summary
Optimized data-driven decision-making by managing end-to-end data pipelines, developing predictive models, and delivering actionable insights for diverse stakeholders.
Highlights
Enhanced data-driven decision-making by gathering and cleaning data from diverse sources (databases, APIs, unstructured formats), reducing data errors by 25% and ensuring data integrity.
Developed and validated predictive data models with over 90% accuracy, leveraging exploratory data analysis (EDA) to identify critical trends and inform strategic decisions.
Optimized data insights through advanced feature engineering and iterative model performance evaluation, enhancing the accuracy and utility of analytical outputs for stakeholders.
Delivered interactive dashboards and comprehensive reports, significantly improving stakeholder understanding and engagement with complex analytics across various business units.
IU School of Medicine
|Data Intern (Healthcare Technology)
Indianapolis, IN, US
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Summary
Improved clinical data management and accessibility by digitizing critical healthcare data, streamlining workflows, and ensuring regulatory compliance within a healthcare technology environment.
Highlights
Digitized liver tumor board data using REDCap, increasing data accessibility by 25% and optimizing clinical decision-making processes through enhanced data representation.
Streamlined complex data workflows, enhancing interoperability and reducing data retrieval time by 20% to support timely clinical insights and data flow management.
Addressed critical technical issues and contributed to the development of robust data governance policies, ensuring strict HIPAA compliance and data quality standards.
Led staff training on updated data workflows and technology platforms, supporting change management initiatives for improved data collection and utilization.
IU School of Medicine
|Clinical Research Data Coordinator and Research Assistant
Indianapolis, IN, US
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Summary
Coordinated clinical research data for complex trials, developing robust data visualization tools and streamlining workflows to enhance operational efficiency and regulatory compliance.
Highlights
Managed comprehensive clinical trial data for Gastroenterology and Hepatology studies, ensuring strict adherence to IRB, HIPAA, and GCP regulatory requirements and data integrity.
Designed and implemented REDCap projects and dynamic SQL/Power BI dashboards, improving data visualization efficiency by 30% to facilitate rapid clinical insights and decision-making.
Collaborated with cross-functional study teams to identify and implement workflow optimizations, enhancing overall operational efficiency by 15% across clinical data management processes.
Authored Standard Operating Procedures (SOPs) and delivered compelling presentations on study findings, directly facilitating data-driven decision-making and data standards compliance.
Government General Hospital
|Clinical Research Assistant and Data Coordinator
Guntur, Andhra Pradesh, India
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Summary
Supported clinical research and data coordination across diverse medical specialties, ensuring data accuracy, regulatory compliance, and patient safety.
Highlights
Documented clinical interactions and provided direct patient care support across various medical specialties, ensuring data accuracy for research studies.
Conducted precise patient screening and eligibility assessments, ensuring strict adherence to study protocols and data collection standards for clinical research studies.
Provided patient counseling on medication use and drug interactions, significantly improving patient adherence and therapeutic outcomes by documenting patient data.
Utilized Clinirex for secure data storage and analysis, ensuring accurate patient records and reporting adverse drug reactions (ADRs) to enhance patient safety and regulatory compliance.
KIMS Hospitals
|Clinical Information Specialist
Hyderabad, Telangana, India
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Summary
Managed patient care and safety initiatives during the COVID-19 pandemic, leveraging clinical knowledge to optimize treatment adherence and patient outcomes.
Highlights
Managed comprehensive patient care as a Duty Medical Officer in the COVID department, ensuring high-quality clinical outcomes and patient safety.
Monitored and reported adverse drug reactions (ADRs) to enhance patient safety and inform treatment protocols, contributing directly to improved patient outcomes.
Provided critical patient counseling and comprehensive discharge planning, significantly improving patient adherence to treatment plans and reducing readmission risks.
Education
Indiana University, Indianapolis
Indianapolis, IN, United States of America
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Master's Degree
Health Informatics
Grade: 3.8
Acharya Nagarjuna University
Guntur, Andhra Pradesh, India
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PharmD
Pharm D
Publications
A Concise Review on Cinnolines.
A short review of bioavailability studies on various drug profiles.
In Vitro Pharmacological Study of Extract of Raphanus Sativus Sprouts
Languages
English
Certificates
CITI - Ethical and Regulatory Aspects of Clinical Research
Issued By
CITI Program
CITI - Clinical Research Coordinator
Issued By
CITI Program
CITI - HIPAA Training
Issued By
CITI Program
CITI - Introduction to the Principles and Practice of Clinical Research
Issued By
CITI Program
CITI - Shipment of Biological Materials
Issued By
CITI Program
CITI - Good Clinical Practice (GCP)
Issued By
CITI Program
CITI - Biomedical Researcher
Issued By
CITI Program
Skills
EHR & Research Systems
Cerner, OnCore, REDCap, Medidata, Oracle, OpenEMR.
Clinical Data Analysis & Management
Patient Eligibility Screening, Data Integrity, Sampling, Longitudinal Data Analysis, Data Flow Management, Data Quality, Data Interchange, Data Mining, Data Representation, Data Acquisition, Database Design, Observed Dataset Requirements, Data Standards, Clinical Data Strategy, Predictive Modeling, Exploratory Data Analysis (EDA), Feature Engineering, Model Performance Evaluation, Interactive Dashboards, Comprehensive Reporting, Data Validation, Data Cleaning, Data Imputation, Data Merging, Data Recoding, Data Scoring, EDC Validation, Data Transfer Agreements (DTAs).
Programming & Tools
MySQL, Python, RStudio, MS Office, Oxygen XML Editor, Excel, Tableau, PowerBI, SAS, R, Shiny, P-SQL, T-SQL, Matlab, Ethovision, Clinirex.
Healthcare Terminologies
ICD-10, HL7, SNOMED-CT, LOINC, RxNorm, NDC, MeSH, Medical Terminology, CDISC, MedDRA, WHODrug.
Regulatory Compliance
Good Clinical Practice (GCP), ICH Guidelines, HIPAA, Clinical Data Management, MQA, CSQ, MHRA, FDA, PhRMA, Privacy Knowledge, Clinical Development Knowledge, 21 CFR Part 11.
Documentation & Processes
Informed Consent Forms, Standard Operating Procedures (SOPs), Data Governance Policies, Change Management, SOP Development, Study Documentation, Protocol Submissions.
Clinical Operations & Patient Care
EHR Assessment, Clinical Decision-Making, Patient Diagnosis, Patient Counseling, Patient Safety Monitoring, Optimizing Delivery of Care, Monitoring Clinical Informatics Systems, Quality Assessments.
Project Management & Collaboration
Project Management, Cross-functional Collaboration, Strategic Planning, Vendor Oversight, Problem Solving, Attention to Detail, Results Orientation, Teamwork, Communication (Written & Verbal).
Therapeutic & Scientific Knowledge
Gastroenterology, Hepatology, Endocrine Disorders, Neuroscience, Psychiatry, Liver Injury, Drug Development, Ophthalmology.
Projects
Liver Injury Study
Summary
Contributed to a multi-center, longitudinal study on drug- and HDS-induced liver injury, focusing on data collection and analysis.
Clinical Decision Support System (CDSS)
Summary
Designed and implemented a Clinical Decision Support System (CDSS) for insomnia within OpenEMR, enhancing clinical decision support capabilities.
Mental Health Data Analysis
Summary
Applied machine learning models to analyze mental health data for medical students, deriving actionable insights for interventions.
Disease Progression and Complications Associated with Endocrine Disorders
Summary
Led a research team to analyze the progression and complications of Type-2 Diabetes Mellitus (T2DM) and Thyroid Disorders, focusing on data analysis and interpretation.