Statistical Programmer Resume Samples

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Statistical Programmers perform a variety of statistical programming tasks required to complete different functions in an organization. Major responsibilities seen on a Statistical Programmer example resume are leading programming staff and assignments, ensuring compliance with standard operating procedures, assisting with statistical quality assurance, and reporting project status to management. Based on our collection of resumes for this role, essential job skills are programming expertise, project management, analytical thinking, computer proficiency, and teamwork. A Bachelor's Degree in computer science or a similar field is usually required.

1

Statistical Programmer

  • Programmed online research surveys using Python, JavaScript, and XML.
  • Cleaned and organized data in Excel and R.
  • Performed statistical analyses in R.
  • Wrote scripts in Python to automate text changes and formatting, saving company time.
Candidate Info
12
years in
workforce
1
year
at this job
BA
Linguistics / English And English / Creative Writing
MA
Linguistics
2

Statistical Programmer Analyst

Work independently in one of the largest CRO global company.

  • Develop and execute statistical analysis plans including generation or validation of tables, listings, and figures and generate reports according to Client requirements.
  • Produce or validate analysis datasets and TFLs for ISS.
  • Develop or validate mapping datasets and derived datasets in multiple projects. Contributed to the development and validation of SDTM and ADaM datasets. This was the first project of its kind for my department recognized by the client (one of the top pharmacy companies) as the CRO of the quarter in 2010
  • Work directly with Lead Data Managers in making data reconciliation reports, developing and reviewing listings and reports.
  • Gave CDISC presentation as part of team for Covance. Attended the CDISC Interchange in MD in Oct. 2007.
  • Extract, transmit and retrieve data from clients and generate SAS datasets including SDTM, or DDT needed for the FDA.
Candidate Info
10
years in
workforce
3
years
at this job
MS
Statistics
MS
Computer Science
3

Quantitative Sciences Intern, Statistical Programmer

  • Constructed simulation algorithm in R to optimize recruitment of the patient population for an analgesic Phase III Clinical Trial
  • Conducted analyses of non-inferiority, cut points for statistical significance, and sample size
  • Generated summary graphics of patient population characteristics throughout recruitment
  • Assisted in validating and replicating dry-run tables and figures from Contract Research Organization (CRO) analysis of trial data
Candidate Info
4
years in
workforce
7
months
at this job
BS
Biological Sciences
MPhil
Genetics
MS
Biostatistics
4

Sr. Statistical Programmer

  • Generated draft and final sets of summary data tables and analyses as part of clinical study reports and ISS/ISE documents for regulatory submission.
  • Wrote project-specific programming code to produce summary data tables and analyses, as specified in statistical analysis plans.
  • Developed utility SAS macros for use in project programs.
  • Validated SAS macros and derived data sets developed by other programmers.
  • Created Submission Datasets in CDISC SDTM and Analysis Datasets in CDISC ADaM standards.
Candidate Info
7
years in
workforce
1
year
at this job
BA
Computer Science
MS
Project Management
5

Senior Statistical Programmer

As a SAS Programmer/Analyst involved in double blind, multi- center randomized Phase III clinical study in the Oncology area.

  • Responsible for database management and SAS programming for statistical analysis, documentation, and reporting.
  • Involved in Statistical summary tables, analysis data sets and patient data listings. Proficient in handling programs, logs, listings, data sets, and transport files.
  • Used SAS/STAT Procedures such as PROC MEANS, PROC UNIVARIATE, and PROC FREQ to develop SAS programs to process clinical trial data on Windows environment.
  • Performed quality reviews and validations of SAS programs (SDTM and ADaM datasets, tables and listings) generated by other SAS programmers. Followed good programming practices and adequately document programs.
  • Reviewed CRFs to make sure all the data collected are uploaded to the database by printing all the variables for each data set.
  • Attended project team meetings, worked with biostatisticians, data managers, and clinical research managers, as appropriate.
  • Provided SAS programming support by generating analysis data sets, tables and listings for important deliverables such as IND annual reports, Investigator Brochure (IB), Annual and Quarterly Safety reports and ad-hoc reports.
  • Generated protocol deviation reports for different studies and data review reports for data cleaning purpose and independent abnormality reports.
Candidate Info
5
years in
workforce
9
months
at this job
6

Contracted Statistical Programmer

  • Designed database structure and created an SQL database for complex clinical data, and allocated the rights for different users.
  • De-indentificated all transcriptions with "gold standard" to protect privacy for patients.
  • Automated above processing with developing a user-friendly system for VIVA to import, export, search, add, delete or edit all the data.
Candidate Info
1
year in
workforce
5
months
at this job
BS
Electronic Engineering
MS
Advanced Analytics
7

Senior Systems Analyst (technical Lead, Business Analyst, Statistical Programmer)

  • Led the selection process and deployment of Clintrial 4, the clinical data management system, a critical capability for the start-up company
  • Integrated the SAS System for statistical data processing, another critical capability for the start-up company
  • Statistical programmer for clinical trials, performing data analysis, mapping, cleaning, and profiling
Candidate Info
18
years in
workforce
2
years
at this job
BS
Natural Resources
MA
Master of Arts
Hdp Developer Apache Pig And Hive
8

Statistical Programmer II

Perform as SP lead and QC lead in multiple studies: interact with biostatisticians, clients and other programmers to fulfill numerous deliveries.

  • Programming on SDTM, Adam SAS and statistical outputs by specification, CRF and SAP
  • Review specification before deliveries to make sure they can be realized in programming.
  • Be proactive to discuss any possible issue before or after data transfers.
  • Check data issue and make document to make sure that they can be fixed by DM department.
  • Manage project budget and propose or try any idea which can make work efficient.
Candidate Info
7
years in
workforce
5
years
at this job
MS
Mathematics
9

Statistical Programmer

  • Used I-Review to extract SAS Datasets, analyze data and generate reports.
  • Designed detailed project plan and schedule to meet the tight regulatory submissions' deadlines.
  • Used SAS programming to generate analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials including FDA requests and submission studies.
  • Made certain that documents and specifications were consistent and comply with company standards by providing input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities.
  • Supported team members of SR and program statisticians in maintaining efficient interfaces with internal and external customers.
  • Used SAS programming to generate PDF simulations of data entry screens for site archives and further refined PDFs by creating page and visit level bookmarks for regulatory submissions to FDA.
  • Provided ongoing support of EDC(Electronic Data Capture) based clinical trials performing quality check of patient profiles.
  • Used EXCEL, ACCESS, Oracle Database and Adobe Acrobat including addition of bookmarks to generate patient profiles.
  • Performed clinical development process using Oracle SQL and PL/SQL.
  • Received Business Excellence Award for meeting challenging deadlines with excellent quality work.
Candidate Info
19
years in
workforce
6
years
at this job
BA
History
MS
Computer Science
MA
Master of Arts
10

Statistical Programmer - Early Clinical Biometrics

  • Used SAS to create CDISC-compliant datasets
  • Developed and validated SAS macros to streamline and standardize departmental workflow
  • Communicated with data managers and statisticians to meet client and regulatory requirements
  • Handled sensitive data in a regulated environment to maintain patient and client confidentiality
Candidate Info
6
years in
workforce
9
months
at this job
BS
Biology
MS
Bioinformatics

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