Job Title: RAVE Study Builder (Global Library)
Location: Seattle, WA or Berkeley Heights, NJ
Duration: 1 year contract
Pay Rate: competitive
Our Client is looking for a RAVE programmer! Responsibilities: * Rave global library and edit check programming (including best practices, efficiencies and reusability)- * Develop, program, test and maintain global edit checks; * Manages library studies and associated objects used for study configuration which have been approved through governance; * Facilitates discussion for identification of objects which will be used for study configuration; * Supports Disease Indication, Therapeutic and Franchise scientists from various therapeutic functions to proactively create new commonly used CRF's and edit checks which could be consumed by study; * Helps Global Librarian to maintain various EDC libraries; * Maintains consistency between Rave Libraries and MDR and/or other standards (if applicable); * Interact with CPs to confirm understanding of client Library for consistent study consumption; * Liaison with the standard governance organization to maintain alignment with the business and proactively look for opportunities to build efficiencies; * Manages risk mitigation, issue resolution and escalation related to Rave Global Libraries; * Provide guidance for resolving Library capability concerns raised Knowledge, Skills & Abilities (KSA's): * Good communication skills-ability to work in a team environment with data managers, medical personnel, clinical monitors, statisticians, programmers; * Strong adherence to timelines and comfortable with escalating deadlines if necessary. * Must be comfortable with speaking up and applying their own experience of best practices. * BS/BA degree or equivalent in a relevant scientific discipline with a minimum of five years' experience. * Experience with one or more of Rave Modules: Coder, CSA, Patient Cloud, Safety Gateway, Site Payments, TSDV desired. * Good communication skills; ability to work in a team environment with data managers, medical personnel, clinical monitors, statisticians, programmers, and medical writers. * Knowledge of FDA/ICH guidelines and industry standard practices regarding programming. * Medical or mathematics/computer science background a plus. * Detailed knowledge and experience in case report form design, data validation. * Knowledge of clinical trial design and basic statistics a plus. * Experience in C# programming a plus.
Sthree US is acting as an Employment Business in relation to this vacancy.