Associate Data Manager

Job Description: Review clinical trial data through CDMS or external data listings to ensure captured data follows protocol and Data Management Plan rules Provide input to and review Data Management Plans for clinical study deliverables Generate queries for internal and external personnel to resolve problematic data Review query responses, resolve discrepancies, and modify databases Support development of CRFs and edit check specifications Participate in user acceptance testing of CRFs, edit checks, and study-specific data listings Prepare and maintain documentation for CRF, edit check, and data listing testingRequirements: Bachelor degree, or international equivalent from an accredited institution, preferably in a technical, clinical, or health-related field, or equivalent combination of education, training and experience 3 to 5 years of practical experience using commercial clinical data management systems and/or EDC products, such as Oracle RDC / Inform, Medidata Rave, and DataLabs Proven experience in all primary job functions may be accepted as an alternative Excellent English verbal and written communication skills Excellent computer skills in a Microsoft Windows environment Proficiency in Microsoft Office Suite tools, including Outlook, Word, and Excel Ability to drive a successful customer experience through positive customer interactions, quality and timely deliverables, and task ownership Strong analytical and organizational skills Ability to work independently and manage multiple projects simultaneously in a fast-paced environment with changing priorities Availability for working hours of 11 AM to 7 PM, Monday-FridayBenefits: Flexible and balanced work arrangements Innovative technologies Continuous learning Skills and opportunities for professional growth .