Clinical Data ManagerIntegrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.Job DescriptionPrincipal Responsibilities:List most complex or difficult parts of job first. Describe scope of responsibilities.Work with Study Teams and partners during study build process to create/maintain the following in CTMS:Study, Country, Site, Contacts, and Institution recordsCreate and set up templates such as Health Authority, IRB/IEC, Financial Disclosure, Subject Visit, Visit/Trip Report, etc.Update system dropdown valuesCreate/Update assignments, configurations, properties, attributes, triggers, and parameters in the system.User administrationImport/Export templatesAdd Payees and study triggersVisit SchedulesSubject deviations/central findingsAny other general study build activitiesTroubleshoot integration errors between CTMS and other applicationsProvide Study build activities for Grants ManagerCreate studyUpload templatesCreate/Add sitesUser administration (send invitations)Any other general study build activitiesAssist with UAT activitiesProvide general business support for CTMS and Grants Manager applicationsCreate/Generate reportsRun SQL queriesSupport Ticket generation/creation and maintenance (tracking of issues/requests)Create/Update reference and training materials/documentationPrincipal Relationships:Reports to Manager, Clinical Trial Management Business SupportInternal interfaces: Study Teams, Champions, Transition Agents, Other support team members, IT.External interfaces: External vendors as necessary (e.g., flexible resource, Medidata vendor).QualificationsEducation and Experience Requirements :University/college degree is required; preferred in health, computer science, business, engineering, or information technologyPreferred prior experience with Medidata CTMS and/or Siebel CTMS or other Clinical Trial Management systems.Knowledge of the Clinical Trial Management processOracle SQL experience is preferred but not required3 - 5 years of professional experience.Additional InformationKind Regards,Sasha SharmaClinical RecruiterIntegrated Resources, Inc.IT Life Sciences Allied Healthcare CRODirect # - 732-662-7964By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy applyI'm interested
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