[Outsource:48283] Required: SAS Programmer with Pharma or CRO exp

Send Resumes to adem@vertigonconsulting.com 

 

Position: SAS Programmer with Pharma or CRO exp

Location: Wilmington, DE

Duration: 6 Months

Our client has an opening for a SAS Programmer who will be responsible for processing clinical data required for the statistical analysis of Phase I – III clinical trials.

Responsibilities:
• Interact with members of the multidisciplinary team to establish project timelines; computerized data validation checks and ad hoc requests.
• Design and implement statistical algorithms and code in conformance with defined programming processes and standard operating procedures
• Ensure that all programs, outputs and documentation are consistent with relevant
• ICH requirements and are conducted in compliance with relevant SOPs.
• Participate in the review, as required, of 'Data Management Plan', 'Statistical Analysis Plan' and other documents essential to the conduct of a clinical trial;
• Work with Clinical Research Organizations, as required, to participate in the oversight and management of programming activities to help ensure timelines and deliverables are met; Implement analysis methods on the collected data and generate analysis data sets and provide summary tables, graphs and data listings using SAS;
• Validate data according to edit specification provided by Clinical Research Organization.  Assess data accuracy and consistency
• Develop standard SAS macros for efficient analyses of clinical data
• Provide relevant information and assumptions to prepare CRO proposal

Requirements:
• BA/BS degree
• 8 years of programming experience using SAS/Base/Macro/GRAPH in the pharmaceutical and/or CRO industries
• Must have very strong communication skills.

Thanks & Regards
 
Adem
Technical Recruiter
Vertigon Consulting
Phone: 201-402-1610
Fax: 732-398-0506
Email: adem@vertigonconsulting.com

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