Hi ,

*Please reply to [email protected] *

Please send me your consultant  updated resume if  they ’re interested for
this position.

*Title:  Clinical SAS Programmer*

*Location: Canton, MI
Duration:  6 Months +
Start Date: Immediate
Interview: Telephone followed by Webex/Skype*
Client: MMS



The candidates will be responsible for the implementation and execution of
various programming needs for the company’s clients in pharmaceutical
industry.

*Responsibilities include:*

   - Provide programming needs to support client’s requirements
   - Work closely with statistical personnel to provide definitions,
   documentation, and review of derived variables needed to produce planned
   tables, listings, and graphs (TLGs)
   - Generate tables, listings and graphs from clinical trial databases
   using SAS
   - Develop, program, verify, validate and maintain clinical trial
   databases and data entry screens using SAS and related software
   - Develop data and programming specifications jointly with other
   programmers
   - Design specific data presentations including creative summary tables,
   graphs and patient listings
   - Assist in preparing the data validation plan based on customers’ needs
   - Review data management guidelines for computer edit/validation checks
   - Adherence to SOPs and programming standards

*Requirements:*

*KNOWLEDGE & SKILLS:*

   - Strong programming and logic skills
   - Hands-on with clinical trials and pharmaceutical development
   - 8 years SAS programming, SAS Base, SAS Macro and thorough knowledge of
   clinical database structures
   - Ability to program data presentations, using programs such as SAS
   procedures
   - Sound experience with data and production of TLGs**

* **EDUCATION & EXPERIENCE:*

   - The candidates must have a Bachelors or Masters degree in computer
   science or related discipline
   - Minimum 8 years experience desired
   - Previous hands-on experience with CDISC and ADaM  are essential
   prerequisites
   - Experience in table and CDISC validation
   - Attention to detail and data mining as needed for data review
   - Experience in the pharmaceutical or CRO industry is preferred
   - Excellent organizational and communication skills are required

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