*Hi All, Please let me know if you have any good resources having all the skills mentioned. Please forward me your consultant updated resume ASAP.* ** *Title : Oracle Clinical Programmer Location : Princeton, NJ Duration : 12 Months Contract*
*Qualifications Bachelor's Degree in Bioinformatics, Computer Science or a related field or equivalent experience Minimum of five years experience creating data objects and procedures in Oracle Clinical 4.5.x Experience in a regulated environment, especially pharmaceutical (21 CFR Part 11) and Phase I-IV studies Strong interpersonal and communication skills; capable of production technical support, training users and writing documentation Team player who can multi-task, work effectively with members of other teams, and communicate productively with clients Good time management and organization skills; the ability to prioritize own work to meet tight deadlines while maintaining the highest standards of work * *Responsibilities Design, create, and validate new studies in Oracle Clinical; this includes data object configuration, and validation documentation Integrate protocol and charter requirements with internal business practices to draft Data Quality Specifications Review study documentation, translate study design parameters into Oracle Clinical data objects Develop validation and derivation procedures that satisfy constraints of study data quality plans Manage validation and deployment of new studies Plan and manage the update and re-validation of amended studies Liaise with Data Management and Project Teams Contribute, in regularly scheduled meetings, ideas and methods for improving the design process Document activities and work according to SOPs. Write clearly and accurately Liaise with Data Managers of RadPharm’s various sponsors to discuss, negotiate, and manage the electronic transfer of clinical data from the sponsor to RadPharm.* ** *Thanks* *Davis Johnson* *davis.john...@catamerica.com* <davis.john...@catamerica.com> *201-257-5081 x 293*--
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