Hi Hope you are doing well
I am Smith, working as a recruiter with Infotree Service Inc. I am currently working on “*Senior ClinicalSAS Programmer Analyst (JREVIEW/LISTINGS)*” position with our reputed client. I will appreciate your response at the earliest, as the managers tend to move fast! *NOTE :* *SEND RESUMES WITH THESE DETAILS , Profiles with all mandatory details would be processed with TOP Priority* *Name (First & Last)* *Contact No.* *Email ID * *Current Location* *Willing to Relocate if need* *Work Visa Status*, *Expiry Date* *Availability * How soon can you join?* *Reason for change* *Are you fine with drug and background check?* *Skype ID* *Last 4 Digit SSN No.* *DOB(Day, Month)* *Higher Education, Year of Completion * *Job Title* *Senior ClinicalSAS Programmer Analyst (JREVIEW/LISTINGS)* *Project Location* *Woodcliff Lake, NJ* *Duration* *12+ months /Contract* *Skills* *Sr. SAS Programmer Analyst (JReview/listings) Data Management Oncology Perform SAS programming to provide data review complex listings/reports to support Data Management, Medical Coding, and other areas of Clinical functions for Oncology trials. Develop programs & graphs in JReview for easier data review and visualization. Develop programs for patient profiles and ad hoc reports to support the clinical teams for Oncology trials. Design and develop SAS macros, applications, and other utilities to expedite SAS programming activities and usage by the Oncology Data Management and other areas of Clinical for data review. Develop and maintain the programs/tools including testing and organizing the SAS datasets, SAS programs and related documentation. Ensure all programming activities and processes performed are conducted according to standard operating procedures and good programming skills. Qualifications: Strong knowledge of JReview and SAS programming skills required in Windows and UNIX environment, with proficiency in Programming in JReview, Graph, Dashboard, SAS/Base, SAS Macros, SAS Graph, SAS/SQL. 5-7 years of experience in programming with clinical trial data and preparing programming and test documentation. Extensive experience of handling external data, such as lab data, PK, and imaging data. Experience of developing programs using JReview. Good understanding of standards specific to clinical trials such as CDISC, SDTM, MedDRA, WHODRUG. Good understanding of relational databases such as ORACLE, Knowledge of the EDC system, InForm, and underlying data structure is a plus. Knowledge of data management process, good understanding of data cleaning process. Strong problem solving skills Able to work independently and a team player, good organizational and time management skills. Capable of communicating technical concepts Good understanding of system development life cycles, GCP, and related regulatory guidelines* Thanks & Regards Smith, Sr. Technical Recruiter Infotree Service Inc. 215 Ann Arbor Rd. Suite 304 Plymouth, MI 48170 734-446-7070 Fax- 734-345-4247 sm...@infotreeservice.com -- You received this message because you are subscribed to the Google Groups "Open Source Erp & Crm" group. To unsubscribe from this group and stop receiving emails from it, send an email to open-source-erp-crm+unsubscr...@googlegroups.com. To post to this group, send email to open-source-erp-crm@googlegroups.com. Visit this group at http://groups.google.com/group/open-source-erp-crm. For more options, visit https://groups.google.com/d/optout.
