Statistical Programmers - New Jersey

Urgently seeking 5 Clinical SAS Programmer for a Direct Client in Plainsboro, New Jersey on a contracting basis. They are one of the Largest Global CRO working with me EXCULSIVELY to expand this team Immediately. Interview are going on right away and I need great statistical programmers to join the team. 5 Contract Opportunities Global CRO6 Month Contracts(extend or hire after 6 months)Plainsboro New Jersey Job Responsibilities: - Ensure quality of personal work and the work of the team when acting as a Lead Programmer. - Carry out all activities according to SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP). - With guidance and sufficient experience prepare and review of Programming Plans. - Participate in the Statistical Programming review of Case Report Forms (CRFs), annotated CRFs, database structures and study related documentation (e.g. data validation guidelines). - Develop and review SAS programs and output as required for the management of clinical trial data, the tabulation of data, preparation of patient data listings, graphical output, creation of derived datasets and statistical analysis of data as specified in the Statistical or Report Analysis Plans. - Develop SAS programs for ad hoc tables and listings. Write, modify, and maintain programs that produce diagnostics and listing for data review in support of Data Management. - Carry out electronic data transfer (both incoming and outgoing). Develop and review programs to ensure the data transfer has been produced to specification. - Review draft and final production runs for projects to ensure quality and consistency. - When acting as a Lead Programmer provide input into resource assessments for programming activities. Qualifications - Bachelors Degree in Statistics, Biostatistics, Computer Science or related, Masters Degree would be a plus- 4-6 year experience as Statistical Programmer, or equivalent experience. - An understanding of the fundamental principles of programming, program development and review. - Experience in the development and review of SAS programs for management and reporting of clinical trial data. - Experience in the development and review of programs to perform electronic data transfer. - Good organizational skills and the ability to prioritize work. - Good time management skills and the ability to work to tight deadlines whilst maintaining the highest standards of work. - Effective communication skills. Please email or call me for more details. APPLY TODAY OR REFER A FRIEND. There are 5 new openings at the moment and interviews are happening!Contact details are on my Linkedin. Search for Paul Dai at Real Staffing Group. ThanksPaul Dai

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