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Online Resumes with "CDISC"
Analyst with good communication and interpersonal skills.
I strive hard to be the best SAS Programmer in the industry using my advanced skill set in SAS and applying my experiences.
Telecommute position providing tables/figures/listings for clinical trials.
Implemented knowledge of ICH GCP and CDISC Standards. Proven organizational skills with the ability to learn quickly; excellent time management, meet tight deadlines; manage multiple tasks and changing priorities while working in a high-pressured environment. Reputable for my attention to detail skills and strong ability to respond and solve problems in real time to fulfill customer expectations. Ability to work effectively...
SAS programming for clinical study reporting, e.g. data and TLG programming; CDISC; PK/PD
Seeking career opportunities in a field integrating Statistics/Biostatistics, Data Mining, Data Modeler, and Decision Science.
Ideal Companies: Pharmaceutical companies; and Health Insurance companies.
I Shivani Pandya, am currently pursuing a master’s degree in the field of Pharmaceutical Administration, at the University of the Sciences, Philadelphia college of pharmacy Please accept this letter and the enclosed resume as part of my application for a position of a Statistical SAS Programmer at your prestigious firm. As a master’s student at Philadelphia college of Pharmacy, I have not only developed good analytical ,...
•Clinical SAS Programmer with over 3 years of experience in designing, developing, testing & validating applications in pharmaceutical and clinical research •Expertise in analyzing and coordinating clinical trial data, generating tables and listings •Proficiency with Base SAS, SAS Macros, SAS/Access, SAS/SQL, SAS/STAT, SAS/Graph, SAS/ODS and SAS/Reports •Knowledge in understanding the PROTOCOLS, CDISC Process (SDTM and ADa...
Dear Sir/Madam, Greetings. I am Krishna, Cheyula-Venkata and I am having 5 years of experience in SAS Programming in Clinical Trials. I am a SAS Certified Base and Clinical Trials programmer using SAS 9. I am a permanent resident here in USA and I can start the new contract in two weeks. I have good experience in clinical trial analysis activities for phase I, II in CVS and CNS therapeutic areas. Solid experience in compl...