求人を保存 検索に戻る 職務内容 求人情報 類似した求人Opportunity to work on diverse projects and interact with global stakeholdersContribute to the establishment of new CRO in Japan企業情報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.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コンタクトEd Marsden求人番号JN-052024-6418109電話+813 6832 8981求人情報分野ライフサイエンス職種治験業界ヘルスケア・製薬勤務地東京23区雇用形態正社員担当コンサルタントEd Marsden担当コンサルタントの電話番号+813 6832 8981求人番号JN-052024-6418109企業タイプ外資系企業勤務形態在宅可・ハイブリッド勤務可
