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Posted over 1 year ago

Title: IRT Project Manager Job Category: Clinical Data Management Job Desc: Job Overview IRT Project Manager Permanent, salaried Remote from anywhere in the U.S. or Canada Responsibilities Responsible for IRT system initial implementation, maintenance, and closure. Ensure comprehensive understanding of requirements and design to provide quality deliverables. Organizes kick-off meeting and team meetings. Coordinates review and sign-off of requirements and release documents. Directs teams during development and testing for initial implementation and updates. Reviews and Approves UAT documentation Manages post-production change controls. Facilitates database lock activities with study team, vendor, and other stakeholders. Coordinates decommissioning and archiving. Advise the team and stakeholders, informing on the processes that will be completed to enable system implementation and updates. Experience Required Minimum 3-5+ years of experience in clinical systems such as CTMS, ePRO, IXRS, EDC or an equivalent combination of education and experience to successfully perform the key responsibilities of the job Strong oral and written communication skills. Experienced project leader and presenter. Able to work both independently and collaboratively across multiple functional areas. Proficiency in understanding complex business requirements and communicating those to technical and project teams. Understanding of Drug Development and Clinical Trial Processes Understanding of Data Management Processes In-depth knowledge of Good Clinical Practices Understanding of Clinical Research System Development Lifecycle Must have sound problem resolution, judgement and decision-making skills. Ability to prioritize tasks effectively and manage multiple projects simultaneously. Education/Qualifications Degree in a mathematical, computing, life sciences, or related discipline Experience Minimum 3-5+ years of experience in clinical systems such as CTMS, ePRO, IXRS, EDC or an equivalent combination of education and experience to successfully perform the key responsibilities of the job Strong oral and written communication skills. Experienced project leader and presenter. Able to work both independently and collaboratively across multiple functional areas. Proficiency in understanding complex business requirements and communicating those to technical and project teams. Understanding of Drug Development and Clinical Trial Processes Understanding of Data Management Processes In-depth knowledge of Good Clinical Practices Understanding of Clinical Research System Development Lifecycle Must have sound problem resolution, judgement and decision-making skills. Ability to prioritize tasks effectively and manage multiple projects simultaneously. Job Type: Full Time C: 17.6