*Hello associates,* *Appreciate your responses with updated word profile, contact details and rate specifications.*
*Full Name:* *Availability:** ** Contact# & E Mail:** ** Current Location:* *Visa Status:* *Rate (You got it for):** ** Willingness to Relocate:** ** Employer details:* *Please find the requirement below and send me the desired profiles of your consultant* ******Please make sure that all the skills in requirement match the consultant profile and send me the profile only at** **[email protected]** ***** *Dear Associates,* *Please find the requirement below and answer ASAP with updated resume and contact details...Thanks* *NEED** **Oracle Clinical Programmer* *We have two openings one strait 12months contract and the other is contract to hire* *Location:** **Princeton, NJ Rate: Open* *Skills:* * * * * *Reports to: Manager, Oracle Clinical Data Base and Application Development* * Overview: This person will design and create Oracle Clinical studies in conjunction with the clinical data coordinators, and study project team leaders. This includes leveraging pre-existing GLib data objects, creation of new objects and creation of validation documents** ** * * 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 various sponsors to discuss, negotiate, and manage the electronic transfer of clinical data from the sponsor 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) * 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* * * *Thanks & Regards, Sam Marshal MNCL Inc. 9810 E. 42nd Street, Suite 223,** **Tulsa,** **OK** **74146** ** Tel: 918-770-0765** ** [email protected] http://www.mncl.net. * * * * *--
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