Hello, Greetings..........
Let me know if you have any one............ *Title:Clinical Data Manager - CDM EDC Skills:Clinical Data Management, EDC, RAD * *Location:Parsippany, NJ Pay rate:Best Rate Length:6 Months * *Job description: *client is an inventor company helping to shape the future and determined to come up with innovations that benefit humankind. Of special importance in this respect are new products emerging from their integrated specialty pharmaceuticals business. client is actively seeking a contract consultant who is experienced at performing clinical data management (CDM) activities and operations. In this critical role, you will: * Participate in or lead the review of Clinical Research (CR) documents (e.g., protocols, reports and statistical analysis plans) by interacting with various CR groups including: Project Managers, Clinical Scientists and Statisticians. * Lead data management activities by working with Clinical Scientists, Clinical Research Associates, Clinical Safety Monitors, Systems Analysts, QC Analysts & Standards Librarian. * Lead the development and define standard and non-standard edit check specifications by utilizing clinical knowledge to create the parameters surrounding data items. * Provide significant input to CRF/eCRF design and address technical issues and edit check programming, as well as contributes to the development of data management reports of clinical data. * Lead Clinical Data Management activities by using Clinical knowledge, data listings and manual review of eCRFs to issue queries and clean data as required. Competencies: * Extensive Clinical Data Management background/experience (minimum 5 Years) required. * Detailed understanding of Electronic Data Capture (EDC) concepts and techniques and of clinical trial principles is required. * Must have hands-on experience with clinical data querying, issues resolution, and coordination of CDM activities. * Excellent verbal and written communication skills and interpersonal skills are required. * Solid understanding of the implications of applicable laws and regulations governing Clinical Research. -- Thanks and Regards, SATYA CAPS innovative Solutions Inc Phone:408/212/0891 408-329-4051 Mailto: [EMAIL PROTECTED] Website: http://capsinnovative.com --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "IT provider" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [EMAIL PROTECTED] For more options, visit this group at http://groups.google.co.in/group/IT-provider?hl=en -~----------~----~----~----~------~----~------~--~---
