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FeaturedAbout Candidate
Dear Sir/Ma’am,
I take this opportunity to introduce myself as Prerna Goyal. I am a Post Graduate in Biotechnology. I have a professional experience of 3 years in conducting non clinical trials as per the OECD guidelines at INTOX Pvt Ltd.
In order to pursue my career in clinical field for more opportunities, I have upgraded my knowledge with following tools:
1. Clinical Research Domain
2. SAS Programming (Base and Advanced)
3. SQL, Macros
4. CDISC, SDTM, ADaM
I am pursuing the professional internship experience through KITE-Ai Technologies in Clinical Data Analytics using SAS programming.
As of today, I have worked on the following projects.
Technical Project Experience
Dataset creation and Listing generation Role-Developer Duration-5 hours Description- Creation of Demographic dataset -Deriving new variables - Assigning new formats - Generation of Excel report using SAS ODS - Creation of listing from demographics dataset Check Outliers Role-Developer Duration-4 hours Description- Outliers creation from raw data -Listing out the duplicate data - Report Generation - Export report using SAS ODS Summary of Demographic tables Role-Developer Duration-5 hours Description- Generation of a Demographics table -Creation of SAS dataset with all counts and percentages -Generation of RTF report using PROC PRINTTO Dataset creation and Listing generation Role-Developer Duration-4 hours Description- Creation of different datasets for inclusion, exclusion and disposition patient’s profile criteria respectively as per the eligibility criteria. - Generation of Log using PROC PRINTTO Listing of Screening Volunteers for Clinical Trials Role-Developer Duration-5 hours Description- Screening of Healthy volunteers for clinical trials - Generation of Log and RTF files using PROC PRINTTO Analysis subject level Dataset Role-Developer Duration-4 hours Description- Analysis dataset creation of SL (Subject Level) - Data Cleaning: Listing out the duplicate data - Deriving new variables - Decoding of Data Summary of Treatment Role-Developer Duration-4 hours Description- Generate summary reports of treatment reports by using procedure tabulate - Generation of Log and RTF files using PROC PRINTTO -Assigning Titles Summary of Medication Role-Developer Duration-3 hours Description- Generate summary reports of concomitant medication reports by using procedure Report - Generation of Log and RTF files using PROC PRINTTO -Assigning Titles Adverse Event Summary Role-Developer Duration-4 hours Description- Incidence of Treatment Emergent Adverse Events by System Organ Class (SOC) and Preferred Term (PT) - Generation of Log and RTF files using PROC PRINTTO Graph Generation Role-Developer Duration-2 hours Description- Generation of Vertical Graph using Proc Gchart
Global Certifications (if any)
Education
Work & Experience
Conducted non-clinical trials as per the OECD guidelines for testing toxicity.