Send Resumes to a...@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: a...@vertigonconsulting.com

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