Sample Resumes CV
http://sample-resumes-cv.blogspot.com CONSULTANT CONSULTANT N AME
SUMMARY Certified SAS Programmer with over eight years of experience in Analysis, design, development, testing and validating the applications. Strong knowledge involving all phases (I-IV) of clinical trials. Worked on SAS/Base, SAS/Stat, SAS/Access, SAS/Graphs and SAS/Macro. Expertise in analyzing and coordinating clinical trial data, generating reports, tables, listings and graphs. Knowledge of CRF-Annotation with respect to various database designs. Knowledge of CRT Dataset creation from clinical trial data, CDISC and MedDRA for regulatory submissions. Reporting computer validation inspections inspections in compliance with 21 Code of Federal Regulations (21 CFR, Part II). Optimize Optimized d performa performance nce using using Data Validatio alidation n and Data cleaning cleaning on Clinical Clinical Trial data using Statistical procedures like PROC FREQ, PROC MEANS, and PROC UNIVARIATE. Involved in writing and updating Standard operating procedures procedures (SOP) for reviews and approvals. Experience in Ad-hoc programming for clinical and data management departments. Knowledge of Programming languages such as C and UNIX SHELL. Highly motivated individual with excellent organizational organizational and interpersonal interpersonal skills. Possess strong ability to quickly adapt to new applications and platforms. Good team leader with strong analytical and communication skills. •
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TECHNICAL SKILLS SAS Tools: Databases: Operating Systems: Languages: Office Tools:
SASV8, V9, SAS/BASE, SAS/ACCESS, SAS/SQL, SAS/MACROS, SAS/GRAPH, SAS/STAT SAS/STAT, SAS/ODS. SAS /ODS. Oracle Clinical, Clin-Trial, SQL server, Oracle7x/8x. UNIX, Linux, Windows98/2000/NT/XP. C/C++, Java, FORTRAN, Matlab, Perl. MS-OFFICE, Word, Excel, PowerPoint, FTP Tool.
PROFESSIONAL EXPERIENCE Client Name, Location Statistical Programmer Programmer Description:
Date - Present
Responsibilities: Ability to write some common macros that are useful across multiple studies. Abilit Ability y to work work on multiple projects simultan simultaneou eously sly and meet the deadlines deadlines as and when required. Perform validation on derived datasets datasets and following the standard standard operating operating procedures during during the validation process. Generate reports either in HTML, PDF or RTF formats according to the client specifications. Worked with Bio-statistician Bio-statistician to analyze the results results obtained from various various statistical procedures procedures like PROC ANOVA, GLM and mixed models. Extensive use of PROC of PROC SQL to perform queries, join tables. Conducted analysis and generated tables, listings and graphs using SAS. Used data _null_ and PROC REPORT to generate the outputs. Involved in helping out the new programmers initially with the i3 standards and project setups. Ability to deliver the TLG’s to the clients in the absence of the lead programmer and participating in off-site meetings. Active participation in monthly departmental meetings and providing the necessary inputs on how to improve the standards. Worked closely with Statisticians, Data managers. Extensive experience in working with people across other sites when required. Environment: SAS/Base, SAS/Stat, SAS/Graph, SAS/SQL, SAS/Macros, SAS/ Access, MS-Excel. • •
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Client Name, Location SAS Programmer/Analyst Description :
Date - Date
Sample Resumes CV
http://sample-resumes-cv.blogspot.com
Responsibilities: Involved in Phase II and III clinical trials by providing required tables and listings. Developed routine SAS Macros to create tables, graphs and listings for inclusion in clinical study reports. Worked on time to event data to generate the required results for the comparator drug and the control drug. Reviewed large macro codes for running the programs. Worked Worked on Kapla Kaplan-M n-Meie eierr macro macro to gene generat rate e the the graph graphs s as per the requir requirem ement ents s for FDA submission. Validating the data sets and comparing the results to that of source programmers output. Timely submissions on the ACM requests. Environment: SAS/Base, SAS/Stat, SAS/Graph, SAS/SQL, SAS/Macros, SAS/Access, MS-Excel. • •
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EDUCATION M.S. in Biotechnology, Texas Tech University, USA
