Sanjeeva Reddy Clinical SAS Programmer

Detail-oriented, organized, and competent Clinical SAS Programmer with 3+ years of clinical experience in utilizing SAS 9.4, to analyze data and draw accurate conclusion. Experienced in CDISC services such as SDTM and ADAM.
Easy methods of teaching for:
Clinical Programming,
Clinical Study design and plans,
Clinical Data analysis,
Clinical Trials,
CRF Annotations,
Programming for Tables, Listings, FIgures,
Study Data Reviewer's Guide,
Analysis Data Reviewer's Guide,
eCTD,
Data Submissions to various Regulatory Authorities,
Clinical Study Report writing,
Safety Narratives, Ec.
Being a Life Sciences Post Graduate, Able teach and clarify each thing distinctively.

Subjects

  • SAS Programming (Beginner-Expert)

  • Statistics (Beginner-Expert)

  • Clinical SAS (Beginner-Expert)

  • CDISC (Beginner-Expert)

  • Tables, Figures, Graphs (Beginner-Expert)


Experience

  • Clinical SAS Programmer (Dec, 2018 - Present) at Genpro Life Sciences India Ltd, Trivandrum, Kerala.
    • Involved in SDTM Specification and Programming
    • Perform Validation of SDTM datasets
    • Generation of TFLs
    • Data Importing and dataset creation.
    • Review of Statistical Plan and TFL shells
    • Preparation of SDRG and ADRG
    • Preparation and Review of Clinical Study Report.
    • CRF Annotations and Edit check programming.
  • Statistical Programmer/ Medical writer (Sep, 2016 - Dec, 2018) at AnaCipher Clinical Research Organization, Hyderabad
    • Developed SAS programs to support Statistical Programming activities
    • Experience working in Integration from multiple sources (ISS and ISE) as well as individual study projects
    • Excellent knowledge in CDISC standards (SDTM, ADAM)
    • Worked with Statisticians to provide SAS programming in analyzing the data, generate reports, tables, listings and graphs
    • Experience in developing the code according to the requirements, following the validation principles.
    • Possess extensive knowledge of developing, modifying and maintaining SAS programs
    • Experience with transforming data in various formats (excel, CSV) into SAS datasets
    • Knowledge of Open CDISC
    • Extensively used different SAS procedures like PROC IMPORT, PROC EXPORT, PROC CONTENTS, PROC APPEND, PROC FORMAT, PROC COMPARE, PROC SORT and DATA _NULL_.
    • Programming Experience with SAS report generating procedures like PROC REPORT, PROC FREQ, PROC MEANS, PROC UNIVARIATE, PROC TRANSPOSE, PROC SUMMARY, PROC PRINT AND PROC SQL.
    • Efficient in understanding the protocol study, study designs, SAP and CRF.
    • Efficient knowledge in Clinical trial data like demographics (DEMOG), adverse events (AE), Labs and vital signs etc.
    • Preparation of the Clinical Study Reports in accordance with the organization SOP and ICH-E3 and sponsor specific formats.

Education

  • Master of Pharmacy (May, 2017 - Jun, 2019) from KGR Institute of Technology and sciences, Rampally, Hyderabad
  • Bachelor of Pharmacy (Nov, 2011 - May, 2015) from St.Peters College

Fee details

    2000-3750/week (US$29.19-54.73/week)