Clinical Trial Project Manager | マイケル・ペイジ・インターナショナル・ジャパン株式会社/Michael Page International Japan K.K.の求人詳細

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更新日 2024-05-08
掲載開始日 2024-05-08

Clinical Trial Project Manager

人材紹介
マネージャーレベル

この求人の取扱い会社	マイケル・ペイジ・インターナショナル・ジャパン株式会社/Michael Page International Japan K.K.
企業名	Global CRO
職種	メディカル/医薬/バイオ/素材/食品 - 臨床開発系医療/福祉/介護 - 看護系（看護師等）メディカル/医薬/バイオ/素材/食品 - 薬剤師
業種	製薬メーカー
勤務地	アジア日本東京都
仕事内容	* Responsible the successful management and communication of all assigned study deliverables, including timeline, budget, resource management. 職務内容 * Coordinate the scheduling, milestones, and progress tracking for clinical projects across all phases. * Provide updates on project status and advancements within a specified geographic area, actively engaging in project review sessions. * Ensure uniformity in study procedures across different regions while identifying any regional variations. * Conduct tailored training sessions for project-specific requirements. * Maintain regular communication with both Global Project Managers and clients. * Lead regional project teams, fostering cohesion, adherence to quality standards, and ongoing training and oversight of daily operations. * Serve as a primary liaison for external contractors and vendors. * Contribute to the refinement and upkeep of project planning documents, essential records, and procedural guidelines. * Supervise the upkeep of both study-specific and corporate tracking systems. 理想の人材 * Strong experience in clinical trial management, particularly within the global CRO industry with a proven track record of successfully managing project timelines, milestones, and schedules. * Excellent communication skills and the ability to effectively report project updates and progress to stakeholders. * A keen eye for detail and the ability to ensure consistency in study processes across different regions while identifying and addressing regional differences. * Demonstrated experience in conducting training sessions, particularly in tailoring content to meet project-specific requirements. * Proficiency in Japanese language, both written and spoken, to facilitate communication with Japanese-speaking stakeholders and team members. * Leadership abilities, including the capacity to manage project teams, foster teamwork, ensure quality compliance, and provide ongoing training and support. * Strong organizational skills and the ability to multitask effectively in a fast-paced environment. * Experience in liaising with external contractors and vendors, as well as contributing to the development and refinement of project planning documents and procedural guidelines. * Familiarity with study-specific and corporate tracking systems, with the ability to oversee their maintenance and ensure accurate data tracking and reporting. 条件・待遇 Great opportunity to contribute to the establishment of a new CRO in Japan Page Group Japan is acting as an Employment Agency in relation to this vacancy.
企業について（社風など）	* Internationally renowned CRO with 30 years of experience in providing expert delivery of pivotal Phase 2 & 3 Oncology, Hematology, Rare Disease, Immunology, Infectious Disease studies expansion worldwide. Currently expanding business within Japan and APAC region.
勤務時間	Flex time available Core hours: 11:00 - 15:00
英語能力	ビジネス会話 (TOEIC 735-860)
日本語能力	流暢（日本語能力試験1級又はN1)
年収	日本・円 900万円〜 1300万円