CURRICULUM VITAE

N S Lakshmi E-mail: adn5y0@r.postjobfree.com

Mobile:+91-812*******

OBJECTIVE

An experienced SAS programmer looking for a position to apply my skillet to contribute to the growth of the company by growing personally.

SUMMARY

Around 2 years of experience in clinical SAS programming.

Essential knowledge of SAS programming techniques and programs especially SAS 9.4.

SAS Certified Advanced Programmer for SAS9 with around two years of experience.

Superior skills in analysing and coordinating data, generating reports, tables, listings, and graphs according to Statistical Analysis Plan, Standard Operating Procedures (SOPs) and departmental guidelines.

Excellent working experience in using various SAS tools like SAS/BASE, SAS/SQL and SAS/MACROS programming.

Good understanding of standards specific to clinical trials such as CDISC, SDTM, ADaM, MedDRA and WHODRUG.

Experience in developing SAS Programs using Procs, Macros and applications for data cleaning, programming, reporting, and documentation.

Peer review of programs and datasets generated by other programmers.

Ability to work independently with minimum supervision in a team environment.

Possess Problem-Solving Skills, Ability to Follow Industry standards and procedures.

Good programming skills in SAS technologies.

Tools and Software Applications

Operating Systems: Windows 98/NT/2000/XP,

Languages: SAS and SQL.

Databases: MS Access 97/2K.

Office Tools: MS-OFFICE, Word, Excel, PowerPoint,

Statistical Software: SAS 9.4

SAS Procs: SQL, REPORT, MEANS, FREQ, SORT, SUMMARY, FORMAT, IMPORT, EXPORT, APPEND, TRANSPOSE, PLOT

PROFESSIONAL EXPERIENCE

Accenture– Bangalore July 2019 - Present

Clinical SAS Programmer

Responsibilities:

Responsible for defining variables, merging datasets, creating derived datasets, data development before processing.

Involved in writing, analyzing and presenting of clinical trial reports for Phase I of clinical trials.

Used SAS to analyze clinical data from CRFs, created SAS data sets for analysis, and generated efficacy and safety reports.

Worked on generating raw datasets on CDISC SDTM standards and analysis datasets on ADAM Standards.

Annotation of CRF as per CDISC –SDTMIG or client requirement.

Proficient in handling various clinical trial domains like Demographics(DM), Exposure (EX), Adverse events (AE), Vital Signs(VS), Concomitant Medications(CM), Disposition(DS), Trail design domains (TDD), ADSL, ADAE etc.

Involved in Statistical programming and validation of Analysis Datasets and Tables, Listings, Graphs (TLG).

Collaborates with the Team Leader to support and ensure the flexible coordination of activities to deliver the assigned projects.

Responsible for checking documentation for standard processes and compliance.

Ensures high quality, timely communication and project information (resources, status of assigned activities, issues) flow to Team Lead.

EDUCATION QUALIFICATIONS

Ph.D (Pharmacology), JNTUH, India (2019)

Master of Pharmacy (Pharmacology), Andhra University, India (2009)

Bachelor of Pharmacy, Andhra University, India (2007)

Declaration:

I hereby declare that the details furnished above are true and correct to the best of my knowledge.

Place: Vijayawada (N S Lakshmi)

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