Reporting APAC in a stand alone position. Be a key member in clinical quality management to ensure effective compliance. Client Details * Global healthcare technology company specialising in digitisation for clinical trials * Supporting over 30,000 clinical trials around globe * International working environment with extensive global collaboration * Hybrid working style Description * Supporting clinical quality management including ICH GCP, clinical regulations/requirements, data management of clinical trials * CSV * Supporting clinical trial processes including eTMF, TMF, SMF * Operate in quality incident management, internal quality system audits, customer audit/inspection Profile * University degree in scientific or related field * High fluency in English and Japanese (non-native level speakers will not be selected) * Clinical quality experience with strong understanding of ICH GCP ideally in the pharmaceutical industry * CSV experience * Exposure to quality systems processes including auditing, root cause analysis, and CAPA development * PMDA inspection experience is preferred * Ability to work independently Job Offer * Competitive salaries and benefits * Great work life balance * International working environment * Hybrid working environment * Work with industry leaders who are solving unmet needs * Great career progression Page Group Japan is acting as an Employment Agency in relation to this vacancy.