Support clinical trial platform technologies, specifically the Rave EDC SystemCollaborate with EDC vendors to translate business requirements into technical solutionsManage Rave EDC FMT meetings, including agenda preparation and minute documentationCoordinate Rave User Access across all studies and URLsEvaluate and assess alternative EDC systems such as VeevaMaintain standard business processes in GDO Systems for regulatory complianceCoordinate Rave upgrades and custom script validation with third-party vendorsLead cross-functional teams in downstream system testing for Rave releasesAct as liaison between R&D stakeholders for Rave access and system enhancementsWork with DTI team to manage enhancements for systems like STAR and DMPProvide technical input for automation and technology adoption in current systemsManage documentation related to Rave User Access, including for acquisitionsConduct risk assessments for evaluating new EDC systemsEnsure confidentiality and professionalism in handling sensitive informationAlign system activities with executive priorities and regulatory needsSkills Required
System Validation, Technical Analysis, Microsoft Office, Regulatory Compliance, Project Coordination