Hi,
I'm Certified Base Programmer SAS 9 holding 2.6 years of experience in clinical SAS Programming. . Experience in designing the Macros and applying in the SAS data program to improve ease and speed of modifications.
Good knowledge in all SDTM
Performed CDISC mapping for clinical trials and classified data into domains
Generating the demographic tables, adverse events and serious adverse events reports.
Extensively involved in Statistical Analysis and reporting of SAS Datasets, reports, tables, listings, summaries according to the Standard Operating Procedures (SOPs) and departmental guidelines.
Excellent analytical, communication and interpersonal skills, and is well motivated to rapidly acquire new skills on the job.
My earlier projects are
Project- 1
Title: Comparative, Randomised, Open-Label, Parallel, Multicentric Study Of Efficacy and Safety Of Cefoxitin Versus Cefuroxime in Patients with Lower Respiratory Tract Infections.
Project- 2
Title: Phase III, Comparative, Randomized, Open-Label, Parallel Multi centric Study of Efficacy and Safety in subjects with Mild to Moderate Bronchial Asthma and Stable COPD.
My technical skills-
SAS Tools: SAS V9.0, 9.2, SAS/MACROS, SAS/SQL
SAS Procedures: All major procedure used clinical trial programming and data validation.
I can handle and complete your project sucessfully in a given deadline.