Use This TemplateProfessional Summary
- 4.5+ years of experience in SAS Programming in CRO and Pharmaceutical Company.
- Aspiring Data Scientist willing to apply machine learning and statistics in real-time pharmaceutical/CRO business problem.
- Passionate about exploring and utilizing Machine Learning Techniques. Ability to understand and translate problems promptly.
- Quick learning abilities to adapt to current technology and market needs.
- Trained and Committed towards apply various machine learning problem solving techniques using R and Python.
- Trained various data science libraries in python like NumPy and pandas with thorough knowledge of python visualization in Seaborn, plotly and matplotlib.
Employment history
Statistical Programmer, Wolf Inc. New Nikole, Nebraska
Feb. 2020 – Present
- Prepare SAS analysis datasets, tables, listings, and figures as per specifications and Statistical Analysis Plan.
- Ability to work on data migration from legacy datasets to standards such as CDISC or any other client specific standard.
- Extensively used client specific SAS standard macros.
- Develop program for dataset integration from various sources or studies under supervision.
- Prepare specifications for CDISC ADaM Datasets
- Prepare, record , verify and maintain complex SAS-based evaluation and reports of clinical trials data.
- Co-ordinate with the client and US-team for clarity of specifications, data issues, outliers, reviews, schedules, etc.
- Perform all the above tasks using standard operating procedures (SOPs) as defined in Quality Management System or the respective client(s) as applicable
Junior Programmer, D'Amore, Stokes and Nicolas. Flatleyborough, North Dakota
Jun. 2018 – Nov. 2018
- Plan and manage programming activities across multiple studies to deliver all data analysis outputs to agreed timelines and quality, (e.g., analysis datasets, tables, figures and listings for regulatory submissions and publications).
- Extensively used company standard macros.
- Review and input into key study documents (e.g. SAP, CRF etc).
- Extensively used company standard reporting tool (HARP-GSK Specific).
- Programming to create ADaM dataset and TLF’s.
- Programming graphs (using PROC SGPLOT/GPLOT) to get better understanding of project progress.
- Preparing study specific documents like ADaM data reviewer’s guide (ADRG) and define.XML and define.pdf version 2.
- Ability to work on data migration from legacy datasets to standards such as CDISC or any other client specific standard.
- Responsible for programming and QC across a study/asset including submission activities adhering to relevant SOPs / policies.
Programmer Analyst 1, Bode-Hackett. Lake Quinton, Louisiana
Mar. 2016 – Apr. 2016
- Experience in SAS Edit checks and client specific reports with Automated Query generation.
- Generating output files in the form of listing, HTML, RTF and PDF formats using SAS ODS.
- Extensively used company standard macros.
- Involved in development and enhancements of SAS programs, and writing code to extract data and perform cleaning and validation.
- 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.
- Create and validate SAS programs for SDTM standard datasets
Education
Eastern California Academy, Legrosberg, Colorado
Bachelors of Engineering, Information Technology, Feb. 2014
Skills
SAS
Experienced
R
Experienced
Python
Skillful
SQL
Experienced
Machine Learning
Skillful
Statistics
Skillful
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More Job Descriptions for :
1
statistical programmer
- Understanding of the study Documents and Data (e.g. Study design and objectives, Endpoints, Sample size, Randomization, Study populations, SDTM, ADAM, TLF, Statistical Analysis, and Safety).
- Reviewed CRF annotations and database data specifications .
- Worked on creation of analysis datasets and tables for DMC, CSR, DSUR, PSUR publications
- Perform analyses defined in the statistical analysis plan as well as ad-hoc analyses as requested.
- Extracting the data from various internal and external databases (Oracle, RAVE, Excel spread sheets) using SAS/ACCESS, SAS/CONNECT, SAS/INPUT, Proc Import etc.
- Worked on FDA Submission studies along with submission activities like CRT package, BIMO listings and SAS pointers in Oncology Therapeutic area for a complex study which involved 7 phases and complex study design.
- Acted as a mentor for new joiners and trainee programmers
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