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Thursday, January 24, 2013

New job Looking for Oracle clinical eCRF programmer // Florham Park, NJ // please send me profiles to suresh@trustek.com // call at 732-393-1313*111

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  • Group: IT Recruiters
  • Subject: Looking for Oracle clinical eCRF programmer // Florham Park, NJ // please send me profiles to suresh@trustek.com // call at 732-393-1313*111

Suresh M posted a job: Looking for Oracle clinical eCRF programmer // Florham Park, NJ // please send me profiles to suresh@trustek.com // call at 732-393-1313*111

"Are you a good fit for this job? Oracle clinical eCRF programmer in Florham Park, NJ Job Category        Clinical and Scientific Job Title              Sr. Database Developer Duration             6+ Months Location:             Florham Park, NJ Hours Per Week     37.5 Hours Per Day      7.5 Duties            :  Provide timely and professional ongoing management of project and clinical trial by developing  and maintaining trial specific database applications, including eCRFs and database specifications, program validation and derivation procedures of various levels of complexity within the clinical database management system in support of in-house and outsourced trials globally for Phase I-IV independently or with  minimal supervision. Major Activities: Develop the eCRF layout and corresponding database according to documented trial specific requirements, using components from existing libraries Create, test and maintain trial specific plausibility and consistency checks Provide data transfer specifications for third party data Maintain and update the eCRF application and its components as required for protocol amendments or required post production changes Develop database specifications, provide guidelines for db setup, review externally created documents, and interact with external partners for outsourced trials Create, file, and maintain appropriate trial documentation Program and test complex procedures, according to documented trial specific requirements,  within the clinical database management system using SQL or PL/SQL Maintain and update procedures as required for protocol amendments or required post production changes and ensure project level consistency Creation & execution of trial design reports based on trial and project metadata Demonstrated experience in the concepts and use of Clinical Data Standards (e.g. SDTM, Novartis standard) preferred.  Understanding of Data Models and implementation for database development Act as a trainer to new or less experienced associates on specific task(s) Subject Matter Expert in functional and technical process and systems Skills              At least 4 years experience in clinical database programming, setup of clinical databases and CRF design, procedure /validation programming, as part of the setup of clinical databases, gained in the pharmaceutical industry or CRO as well as the following: Strong knowledge of SQL or PL/SQL. Strong OC/RDC experience Knowledge of clinical data management systems and/or relational databases as applied to clinical trials Attention to detail, quality, time management and customer focus. Ability to translate technical concepts for non-technical users in the areas of clinical database design and procedure development Strong verbal and written communication skills to work with our global partners and customers Ability to train and supervise junior Database Developers (eCRF Study Builder/ Procedure Developer) Keywords Education           University or college degree in Life Sciences, Mathematics, Computer Science, Medical Informatics, or equiva... http://bull.hn/l/Z7MG/6"

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