Clinical SAS DM Programmer - New Jersey

Hello

Happy New Year and Best Wishes! Hope all is well for 2013.

I have a NEW Contract Opportunity for a Clinical SAS Programmer for a Major Pharmaceutical Company in North New Jersey. 12 month contract with possible extension. Apply Today and come join a fast growing company.

12 Month Contract
Clinical SAS Programmer (Data Management Group)
Major Pharmaceutical
Northern New Jersey

Sr. Clinical Programmer

* Perform SAS programming to provide data review complex listings/reports to support Data Management function for Oncology trials.
* Develop programs to provide patient profiles and ad-hoc reports for data review to support the clinical teams.
* Participate in review process of study documents such as the annotated CRFs/eCRFs.
* Program data edit checks, as necessary, to facilitate Data Management's data cleaning activities.
* 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 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 practice

QUALIFICATIONS:
* Strong SAS programming skills required in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SAS/AF, SQL;
* Seven to 10 years of experience in programming with clinical trial data and developing programs ,testing, and documentation;
* Experience in handling SDTM mapping, related data structures, and programming to create SDTM data sets;
* Extensive experience of handling external data, e.g., laboratory data, PK, ECG, etc.;
* Knowledge of developing reporting or other systems using SAS;
* Knowledge of data management process; Good understanding of data cleaning process;
* Good understanding of standards specific to clinical trials, such as CDISC, SDTM, MedDRA, WHO DRUG;
* Good understanding of relational databases, e.g., ORACLE; Knowledge of the EDC System, InForm and underlying data structure is a plus;
* Knowledge of using JReview is a plus;
* 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.

Please email me if you have any questions. APPLY TODAY by sending me an updated resume ASAP.

Thanks
Paul DaiTo find out more about Real Staffing please visit www.realstaffing.com