From: Christian O. <yd...@jo...> - 2006-10-21 19:17:36
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<!DOCTYPE html PUBLIC "-//W3C//DTD HTML 4.01 Transitional//EN"> <html> <head> <meta content="text/html;charset=ISO-8859-1" http-equiv="Content-Type"> </head> <body bgcolor="#ffffff" text="#000000"> <img alt="" src="cid:par...@jo..." height="396" width="852"><br> You will work within specified timeframes on multiple projects in a commercial setting.<br> Appropriately documents and validates statistical programs.<br> Surface Plasma Resonance.<br> Research and implement appropriate statistical and machine learning methods. Work with Business Analysts, gather functional requirements, and ensure that supported data model conforms to these requirements as well as modeling standards. Define and implement data warehouse transformations; develop and manage ETL processes for warehouse and data mart build and maintenance.<br> You will work within specified timeframes on multiple projects in a commercial setting.<br> These staff provide the high level product knowledge and skills to present The company Informatics products to potential and existing customers. Determine specific needs of end users; design and implement software, etc.<br> Report to the Regulatory Affairs Director.<br> Adhere to the regulatory bodies - and coordinate between US, EU and UK. Experience in writing and executing validation documentation.<br> Degree in Chemistry or related discipline. Apply innovative techniques in designing and unit testing of the product.<br> Independently programs in SAS to generate tables, listings and graphs for clinical study reports and submissions of data to global regulatory agencies. Redesign graphics in . In this role you will be responsible for study design, protocol preparation, in-life study conduct and monitoring, data evaluation and interpretation and reporting.<br> Provide support and maintain released data models and existing ones. Analyse swab and rinse samples. CW agent detection and analysis of data. Knowledge and experience of computer programming, databases, process control.<br> Your duties will include the design, implementation, and testing of key software components of the Verseon proprietary drug discovery platform. Surface Plasma Resonance.<br> Comprehensive understanding of pathophysiology of diseases and molecular mechanism especially in metabolic, cancer biology, respiratory inflammation will be advantageous. Research and implement appropriate statistical and machine learning methods.<br> Define and implement data warehouse transformations; develop and manage ETL processes for warehouse and data mart build and maintenance. Appropriately documents and validates statistical programs.<br> net and other solutions. Develop medical SOPs.<br> net and other solutions. Plan and document testing tasks.<br> Requirements: Strong experience in an applications development environment programming with SAS software. Plan and document testing tasks. Liaise with physicians and attend meetings.<br> You will co-ordinate all communications with the technical team, Quality Assurance and the Sponsor.<br> Adhere to the regulatory bodies - and coordinate between US, EU and UK.<br> <br> </body> </html> |