Dear Business Partner, My client is looking for a SAS Clinical Statistical Programmer - Green Card or US Citizens only - C2H. Please share your consultants suitable resumes with me on my ID: [email protected];
Job Title: SAS Clinical Statistical Programmer Location: Wayne, PA Duration: 6+ Months Contract to Hire Additional Job Details: Only candidates that will be considered are those that have either valid US Citizenship or US Permanent Residence for work authorization. Description/Comment:- Minimum of a Bachelor’s degree Minimum 8 years SAS programming experience in the pharmaceutical, biotechnology, and/or contract research organization industries The Clinical SAS Programmer creates SAS programs in support of sponsor’s clinical trials according to SOPs and guidelines. This programmer will create, document, validate, process, and maintain statistical programs and macros that generate analysis datasets, tables and graphics with high quality per agreed timelines. For the project lead position, the Clinical SAS Programmer will provide direction and oversight to programmers in creating sponsor deliverables. Act as lead programmer to write SAS programs that produce analysis datasets (ADaM) and analyses specified (ADaM) in the Statistical Analysis Plan Act as quality control programmer to validate SAS programs that produce analysis datasets and analyses specified in the Statistical Analysis Plan Assist the Manager of Clinical programming in overseeing the daily tasks associated with clinical programming and subsequent analysis to ensure sponsor deliverables are created per agreed timelines and to high quality standards. Ensure SAS programs adhere to SOPs, guidelines, and specifications Ensure SAS program output matches the requirements of the Statistical Analysis Plan Consult with managerial, statistical, data management, DIS, and medical writing personnel to clarify program intent, identify problems, and suggest changes. Design and/or review database structure Create derived-analysis datasets Execute analyses specified in the Statistical Analysis Plan (SAP) or Report and Analysis Plan (RAP) under the guidance of the project statistician Take instructions and perform tasks as necessary as directed by reporting manager Ensure specifications and documentation are correct and complete Work with other team members to ensure outputs are correct and complete Organize, plan, and prioritize work to develop specific goals and plans to prioritize, organize, and accomplish project objectives Analyze information and evaluate results to choose the best solution and solve problems. Preferred Skills:- Extensive knowledge of Base SAS, SAS/GRAPH, SAS/STAT, and ODS Experience as a Lead Programmer managing the daily activities of the Programming team Experience in managing external client interactions and relationship building Experience working with heterogeneous data structures Ability to work independently and adept at managing multiple competing tasks Good understanding of clinical data and pharmaceutical development Knowledge and experience using SDTM and ADaM,data structures Knowledge of FDA and ICH guidance Knowledge of clinical trial conduct and the data and reporting requirements for clinical trials Knowledge of SAS programming techniques needed to produce outputs in accordance with specifications Thank you for your time and look forward to work with you. """""""""""""""""""""""""""""""""""""""""""""""""""""""""""""""""" Regards, David Johnson|Recruiting Specialist| Desk: 609-423-4881 Email: [email protected] This email message, including any attachments, is for the sole use of the intended recipient(s) and may contain confidential and privileged information. Any unauthorized review, use, disclosure or distribution is prohibited. If you are not the intended recipient, please contact the sender by reply e-mail and destroy all copies of the original message. -- You received this message because you are subscribed to the Google Groups "project managment" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/project-managment. For more options, visit https://groups.google.com/groups/opt_out.
