Clinical Data Analyst III

Clinical Data Analyst IIIContractCompany DescriptionIRI believes in commitment, integrity and strategic workforce solutions.Integrated 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.We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success.Job DescriptionClient: Direct ClientLocation: Raritan, NJJob Title: Clinical Data Analyst III/Clinical Data Manager III PositionDuration: 1 year+Job responsibilities:• Clinical Data Analyst is responsible for CTMS and Grants Manager study build, maintenance, and support activities.• Work with Study Teams and partners during study build process to create/maintain the following in CTMS:• Study, Country, Site, Contacts, and Institution records• Create and set up templates such as Health Authority, IRB/IEC, Financial Disclosure, Subject Visit, Visit/Trip Report, etc.• Update system dropdown values• Create/Update assignments, configurations, properties, attributes, triggers, and parameters in the system.• User administration• Import/Export templates• Add Payees and study triggers• Visit Schedules• Subject deviations/central findings• Any other general study build activities• Troubleshoot integration errors between CTMS and other applications• Provide Study build activities for Grants Manager• Create study• Upload templates• Create/Add sites• User administration (send invitations)• Any other general study build activities• Assist with UAT activities• Provide general business support for CTMS and Grants Manager applications• Create/Generate reports• Run SQL queries• Support Ticket generation/creation and maintenance (tracking of issues/requests)• A university/college degree is required; preferred in health, computer science, business, engineering, or information technologyQualificationsQualifications and Experience Required• Preferred prior experience with Medidata CTMS and/or Siebel CTMS or other Clinical Trial Management systems.• Knowledge of the Clinical Trial Management process• Oracle SQL experience is preferred but not required• 3 - 5 years of professional experience.Additional InformationThanks!!!Warm Regards,Amrit SinghClinical RecruiterIntegrated Resources, Inc.