A Statistical Programmer is a type of statistician who concentrates on creating computer software that collects, analyses, and reports information from large databases. A well-written Statistical Programmer Resume indicates the following core duties – performing activities with minimal supervision, overseeing the statistical programming personnel; developing a program for dataset integration from various sources or studies under supervision; preparing programming documentation, preparing resource plans as needed, assisting in quality control and auditing all statistical programming deliverables; participating in CROs selection and monitoring SR trial activities, providing input on entire process enhancement initiatives, and providing input on entire process enhancement initiatives.
Those seeking to make a career in this line should demonstrate the following skills – highly proficient with using computers and programming languages, the ability to use all types of software, high level of precision and accuracy, skillful in communicating complex ideas in a simple way; and a good understanding of advanced topics such as math and statistics. While entry-level posts need only a degree, some specific-niches require a master’s degree in statistics.
Headline : Highly qualified Statistical Programmer with experience in the industry. Enjoy creative problem solving and getting exposure on multiple projects, and I would excel in the collaborative environment on which your company prides itself.
Skills : Planning, Developing, Supervising.
Description :
Responsible for the statistical programming of preclinical and clinical trials as well as for ISS/ISE in collaboration with the biostatisticians and data management.
Efficient programmed for statistical analysis of phase III clinical trials (including SDTM datasets, ADaM datasets, FIRs and TFLs).
Developed programming specifications for analysis datasets, pooled datasets, and deliverables in consultation with the statistician.
Propered QC documentation for all programs and outputs.
Supported quality control and quality checks of deliverables.
Supported by biostatisticians in SAP development.
Wrote programs for Adhoc requests for interdepartmental reviews mainly for Biostatistics, Medical Writing, etc.
Experience
5-7 Years
Level
Executive
Education
MS
Statistical Programmer Resume
Objective : As a Statistical Programmer, responsible for Reviewing all customer issued specifications, drawings, and ECO’s, Reviewing internal engineering drawings and specifications, and also Interpreting drawings/specs.
Skills : SAS SKills, Communication Skills, Multitasking.
Description :
Planned and executed the transfer and analysis of data for safety/efficacy monitoring boards/independent data monitoring committees.
Developed Safety Update Reports, Periodic Benefit-Risk Evaluation Report, Investigators brochures.
Contributed to the development of best practices to improve quality, efficiency, and effectiveness.
Produced and maintained technical database standards and programming specification documents.
Contributed to the statistical programming deliverables for regulatory submissions, including specification and delivery of overview databases, outputs, and response to regulatory questions.
Contributed to the delivery of the Clinical Study Report, Study Data Tabulation Model/Analysis Data Model databases and Tables, Figures and Listings through both internal and external delivery models.
Communicated effectively in the English language in person, by phone, and in writing.
Experience
2-5 Years
Level
Executive
Education
MS
Statistical Programmer Resume
Headline : Statistical Programmer with 5 years of experience. Currently working as Statistical Programmer for Phase I-IV Oncology studies in Gilead Sciences, Inc.. Previously worked as Statistical Associate Consultant in Indiana Statistical Consulting Center. Good oral and written communication skills. Goal- and action-oriented. Work productively independently as well as collaboratively.
Skills : SAS, R Programming, Data Analysis.
Description :
Mapped raw data to CDISC SDTM standards, and create safety and efficacy analysis datasets using CDISC ADaM standards, and create annotated Case Report Forms (CRFs) and mapping specifications.
Programed Tables, Figures, and Listings (TFLs), in accordance with the Protocol and Statistical Analysis Plan (SAP).
Utilized controlled terminology and coding dictionaries such as MedDRA or WHODrug.
Performed data checks as needed to understand structure and content of data.
Created the item 11 CRT package (define.xml) using specific SAS macros.
Interacted with Clinical Data Management (CDM) to resolve data issues.
Interacted with Biostatistician to develop SAP.
Experience
5-7 Years
Level
Executive
Education
GED
Statistical Programmer Resume
Headline : Certified Statistical Programmer with five (5) Years of Experience within the pharmaceutical industry/CROs. Experience in analysis and reporting in clinical trial data analysis. Strong Experience in SAS data step programming for data manipulation, processing, quantitative and qualitative analysis and report writing.
Skills : Statistical Analysis, SDTM Programming, ADaM Programming.
Description :
Understood the business requirements.
Gathered the requirements from user - Creating Reports.
Extracted data from different databases.
Modified data using SAS /BASE and Macros.
Generated safety and efficacy analysis datasets based on dataset specifications using CDISC SDTM, ADaM standards Developed reports using Proc Report and Data _Null_.
Extensively worked with SAS Macros.
Performed QC Programming for derived datasets and TLF's using proc compare and manually as per SAP shells.
Experience
5-7 Years
Level
Junior
Education
Bachelor Of Science
Statistical Programmer Resume
Headline : Seeking a Statistical Programmer profession with an outstanding career opportunity that will offer a rewarding work environment along with a winning team that will fully utilize management skills.
Generated Ad-hoc reports and programs for clients within tight deadlines in accordance with client specifications and comments.
Wrote and modified and updated programs using Macros, Proc SQL, and Data step programming as per comments (definitions) sent by the client.
Responded to statistical and non-statistical questions from Medical Writing.
Wrote efficient SAS 9.2 programs to analyze large national health datasets.
Utilized Omniture web analytics metrics to gain insight into questionnaire database user activity.
Manipulated data sets by using RETAIN, ARRAY, DATA _NULL_, SAS Functions, etc.
Used Sorting and Merging techniques on the raw data sets for value-added data preparation, to get the required Reports or Analysis data sets.
Experience
5-7 Years
Level
Junior
Education
BA
Statistical Programmer Resume
Headline : Over six years of experience as a Statistical Programmer with good knowledge of advanced statistical methodologies applied in Pharmaceutical and Biotech industries. Expertise in analyzing and reporting various phases (Phase I-IV) Of Clinical Trials using tools like Base SAS, SAS/STAT, SAS/GRAPH, SAS/SQL, SAS/MACRO, SAS/ACCESS, and SAS/ODSin UNIX and Windows environment.
Provided leading-edge health care through the diagnosis and treatment of patients suffering from rheumatologic and related disorders.
Generated statistical analysis files, tables, listings, and graphs for Phase III drug trial studies.
Collaborated with Statisticians, Data Manager, and other SAS programmers to provide ad-hoc and routine analyses and reports with regards to the assigned projects.
Supported Data management in data creation/transfers and integrity checks Imported external files like Excel files, text files, and Database files into SAS data sets using INFILE, LIBNAME, PROC IMPORT, SAS/Macros, and SAS/Connect, etc.
Used various procedures such as Proc Means, Proc Freq, and Proc Univariate to check assumptions and produce initial analyses.
Worked with different clinical trial data like Demographics, Medical History, Vital signs, Adverse Event (AE), Physical examination.
Created SAS data sets by extracting data from various sources and prepared them for statistical analysis.
Experience
5-7 Years
Level
Executive
Education
BA
Statistical Programmer Resume
Headline : Responsible for Contributing to or lead the statistical programming thinking, analysis, and reporting to relevant groups in product and study teams, and also Developing a standard methodology to improve quality, efficiency, and effectiveness.
Worked collaboratively, effectively, and productively in diverse organizational structures.
Worked independently, take initiative, and complete tasks to deadlines Delivering Excellence, Serving Customers, Accountability and Ownership, Global and Cross-Functional Communication.
Worked in a team-oriented, collaborative environment.
Worked positively within a continually changing environment.
Effectively prioritized and executed tasks in a high-pressure environment.
Contributed to the Development Safety Update Reports (DSUR), Periodic Benefit-Risk Evaluation Report (PBRER), Investigators brochures (IB).
Experience
5-7 Years
Level
Executive
Education
MS
Statistical Programmer Resume
Headline : To establish a long-term career in a company where I may utilize my Statistical Programmer professional skills and knowledge to be an effective Statistical Programmer and inspiration to those around me.
Skills : Excel, Access, Developing.
Description :
Acted as validation programmer for a project to coordinate all study activities and provide input to project documentation as appropriate including review of statistical analysis plan and CRFs.
Ensured that data and programming code meet CDISC standards in both SDTM and ADaM model as per (SDTMIG 3.1.2 and ADaM IG v1.0).
Performed developer testing, independent programmer testing, and user acceptance testing on internally written programs.
Ensured that datasets, tables, figures, listings, and statistical outputs are produced in an efficient manner, following Programming procedures and standards.
Worked collaboratively with Biostatisticians, Statistical Programmers, Clinical Data Managers, and other Clinical, and Project Management team to meet project deliverables and timelines for clinical data analysis and reporting.
Informed internal and external project team members of statistical programming requirements, deliverable status, and resource needs.
Reviewed statistical analysis plans for all assigned studies and provides comments to study biostatistician.
Experience
5-7 Years
Level
Executive
Education
MS
Statistical Programmer Resume
Headline : Seeking a Statistical Programmer position, responsible for Serving as the core project team member to design and specify the overall approach to projects programming tasks, Supporting statisticians with computer programming tasks.
Generated Tables, Listings, and Graphs using SAS Tools - SAS/Base, SAS/Macros, SAS/Graph, and SAS/SQL.
Developed utility macros for several studies and created tables and figures by using macros.
Developed a macro to extract the data from the oracle clinical database and developed a standard macro for the adverse event table.
Worked with all kinds of Clinical Trials data such as Demographic data, Adverse Events (AE), Serious Adverse Events (SAE), Laboratory data (Lab data), and Vital Signs.
Developed SAS macros to create Tables, Graphs, and Listings for Clinical Study Reports.
Prepared data listings for data management Created efficacy tables by using Analysis of Variance (ANOVA), Proc REG, Proc CORR, Proc GLM, and Proc Mixed.
Produced SDTM data sets from the existing SAS data sets as per the SDTM 3.1 specifications.
Experience
5-7 Years
Level
Executive
Education
MS
Statistical Programmer Resume
Summary : Detail-oriented, dedicated, and highly motivated Statistical Programmer with 15+ years of professional experience. Solid analytical, communication, organizational, and critical thinking skills. Expertise in data set building and checking and performing data analysis for the fields of medical research and toxicology.
Skills : SAS Programmer, SQL, Statistical Analysis.
Description :
Durbin served as the project supervisor of a grant with the CDC's National Immunization Program (NIP).
Coordinated and supervised the creation and maintenance of an internet-based data link connection between Emory and CDC.
Performed simple, linear, multivariate, and logistic regression analyses utilizing SAS and were responsible for the publication of results.
Supported the project through detailed database analysis/administration through SAS, SUN, Access, UNIX, and other platforms/systems.
Created analysis data sets using the ADaM model.
Used Output Delivery System (ODS) facility to write safety and efficacy reports directing SAS output to RTF and PDF.
Worked on early development studies Worked on PK/PD analysis Worked on CDISC.
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