Dedicated data analyst with over 3 years of experience in market research and data visualization.
Applied statistical techniques and tools to interpret complex datasets for decision-making.
Created detailed dashboards and reports using Excel and Tableau to communicate findings effectively.
Conducted surveys and data collection to evaluate market trends and customer preferences.
Coordinated multiple research projects, ensuring timely delivery and quality standards.
Cognizant Technology Solutions ( Canada )
Development and validation of safety datasets like Subject level information (ADSL), Adverse Events (ADAE), Concomitant Medication (ADCM), Vital Signs (ADVS) and Laboratory (ADLB)., Responsible for the development, review, validation and execution of SAS programs to generate ADaM to be included in reports for submission to regulatory agencies., Create statistical outputs to be used in support of final reports and other clinical publications, support systems to produce electronic regulatory submissions., QC SAS programs for Datasets, Tables, Listings, and Figures following QC procedures., Have in-depth knowledge on understanding the data and standard documents required to generate the datasets and TLFs.
Cognizant Technology Solutions ( India )
Worked in Phase I - III study in therapeutic areas like Growth hormone, Insulin and Devices, Hemophilia and Obesity to evaluate the safety and the efficacy of the drug., Created SAS programs to develop and validate the safety and efficacy related Tables, Listings and Figures., Involved in development and validation of safety datasets like Subject level information (ADSL), Adverse Events (ADAE) and Concomitant Medication (ADCM) and Vital Signs (ADVS)., Validated ADaM datasets extensively by independent programming., Worked on Drug Safety Update (DSUR), Periodic Safety Update (PSUR), Risk management plan (RMP) and Bioresearch Monitoring Program (BIMO)., Worked with the cross-functional team with medical writers, statisticians, Data management team., Used the SAS auto call facility, while creating the macro and storing compiled macros SAS/Macros.
Post Graduate Diploma
Bachelor of Engineering
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Cognizant Technology Solutions ( India )
Incorporation of Non-Infolink sources into the reporting mart., To create processes that will import Non-Infolink sources into the reporting mart in the form of staging tables and to build materialized views that link tables to various dimensions., As per the client’s specification document, the raw data were converted into SAS tables and were uploaded onto Oracle database., Developed efficient, well-documented, readily comprehensible and modifiable SAS code using SAS/ Base and SAS/ Macro facility., Analyzing various tables using Data manipulation techniques like merging, appending, concatenating and sorting., Prepared new Datasets from raw data files using Import Techniques and modified existing datasets using Set, Merge, Sort, and Update, Formats, Functions and conditional statements.
Tata Consultancy Services
The client’s oracle clinical data was transformed into GDM (Generic Data Model) datasets are SAS datasets., The clinical reports were generated using GDM datasets. We had to ensure that reports formats are set up to produce outputs as required by the Client’s specifications., Analyses of client system errors reports and identify corrective action and recommends solutions through issue log to the Roche point of contact., Monitored data and reports produced to determine quality and accuracy of the GDM., Analyzed data problems and reports to Roche point of contact through issue log., Tracked and followed up on all issues raised by them in the Issue log., Validated outputs produced by other safety data analysts to ensure they meet required specification and documents validation results.
SIRO Clinpharm Pvt Ltd.
Mapping of legacy data to the client’s data standards. Developing / maintaining preprocessing macros in BASE SAS to map the legacy data to the client’s data standards., Generating Standard Safety Reports in CDARS., QC of the mapped data with the legacy data., Analyzing data and producing tables and listings for safety analysis in specified formats for submissions or for other purposes., Worked on the summary of clinical data like Demographic, Adverse Events (AE), Serious Adverse Events (SAE), Adverse Events by System Organ Class and Preferred Term, Related Adverse Events and Adverse Events Leading to Discontinuation., Proficient in understanding Study Protocols, SAP (Statistical analysis plan), and CRF.
