Wednesday, March 8, 2017

Contract Position--> SAS Programmers in Woodcliff Lake, NJ

Hello,

 

Hope you are doing great today!!!

 

This is Anurag Srivastava from IDC Technologies.

We have a job opportunity available for the position SAS Programmers in Woodcliff Lake, NJ. Please go through the job description below and let me know if you are available and interested for this position. Please reply me back with your most updated resume.

 

Position: SAS Programmers

Location: Woodcliff Lake, NJ.

Duration: 12+ months

Interview process: Phone, then face to face. NO SKYPE INTERVIEWS!

 

 Main duties/responsibilities: 

Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: analysis datasets, statistical tables, figures, listings, Integrated Summaries of Safety (ISS), Integrated Summaries of Efficacy (ISE), DSUR, PSUR, IB, progress reports, electronic submissions and other internal and external requests (e.g., publications).

Accessing and converting data to SAS from Database management system and PC file formats (e.g., MS Excel, text files).

Working with external vendors in order to develop or monitor the content and structure of SAS data sets.

 

Strong technical skills and Oncology experiences supporting submissions are required. 

Strength in ADaM datasets are critical

Experience required: 

  • Minimum 3 years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. 6+ years' experience preferred. 
  • Some project experience in a pharmaceutical programming environment or demonstrated significant leadership of SAS programming activities in a clinical pharmaceutical environment. 
  • Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office.
  • Knowledge of SDTM and ADaM standards. Strength in ADaM datasets are critical
  • Proven experience with UNIX and Windows operating systems. 
  • Understanding of the software development life cycle. 
  • Understanding of FDA guidelines. 
  • Good organization, time management and attention to detail skills needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality. 
  • Applies good judgment and demonstrates initiative to resolve issues. 
  • Strong verbal, written and interpersonal communication skills needed to work effectively in a team environment, managing that team as required 

Minimum of Bachelor's degree in Statistics, Computer Science, Mathematics, or a related science discipline.

Strength in ADaM datasets are critical

MORE PHARMA INDUSTRY NOT CRO.

Strong technical skills and Oncology experiences supporting submissions are required. 

Knowledge of SDTM and ADaM standards

 

 Anurag Srivastava

IDC Technologies, Inc
Work: 408-668-8346
Mailto:
anurag.sri@idctechnologies.com
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