System Set-up Analyst [Multiple EMEA Locations Considered]

The System Set-Up Analyst (SSA) ensures the technology set-up at a clinical trial’s outset supports the profitability of the trial, ensures quality delivery, and maximizes the efficiency of operational resources assigned to the trial. For assigned trials, the SSA has global responsibility for the design, requirements gathering, requirements documentation, and the accountability for the implementation of technology to meet the specific needs of the assigned trials. The SSA will work with Parexel’s standard technology, and if non-standard technology is required, the SSA will escalate to their assigned Client Technology Partner.

Key AccountabilitiesServe as the single point of contact with the project team for trial-level technology, and data integration solutions, covering CRS, PI, IT, and technology third party vendors Define and document requirements for the trial technology Be accountable for all technology set-up for assigned trials; this includes working with colleagues across departments who have specific responsibilities for part of the set-up Coordinate the teams responsible for delivery of the technology for a trial, including design, using standard components, based on customer requirements, planning and coordination of delivery of the technology and input to the overall project plan Ensure the quality, timeline and budget related to the trial technology meets the project requirements Escalate requests or requirements for non-standard technology to the assigned Client Technology Partner Set-up trial technologies if appropriate Ensure project team satisfaction of the trial technology solution Train and mentor more junior System Support Analysts Stay updated on technology and clinical trial process developments and requirements within Parexel

QualificationsCommunicationExcellent verbal and written communication skillsStrong customer focus (internal and external)Coordinating global virtual teams around trial technology set-upProven ability to manage independently competing priorities with attention to detailExperience in team coordination and requirements gatheringAbility to motivate and work effectively with virtual teams within different cultural environmentsAbility to negotiate and influence in order to achieve resultsTechnical and data standard experienceExperience in clinical trial systems (e.g, CTMS, EDMS, EDC, IVRS, reporting tools) and in configuration of these systemsDevelop detailed awareness of CRS, PI and external vendor software and tools with practical knowledge of how these applications work, and provide efficiency to operationsDemonstrated adeptness in learning new systems and function in an evolving technical environmentAwareness/experience in the needs and use of data standards in clinical trial environment; if possible knowledge/experience of data standards such as CDISC SDTMBusiness processIn depth understanding and experience of clinical trial processesKnowledge of SOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.GeneralCommitment to quality and quality management.Commitment to operational efficiencyFlexibility to change.