IQVIAは、ヒューマンデータサイエンスの先駆者として、医療・ヘルスケアの未来を切り拓く革新的なソリューションを提供しています。世界最大規模の医療・ヘルスケア関連データを基盤に、人・データ・サイエンスを融合させ、未だ満たされない治療ニーズへの対応、新薬・医療機器の開発支援、規制・コンプライアンス対応、持続可能な医療システムの推進など、患者さんをはじめとするすべての人々のために、より良い未来の実現を目指しています。
世界100以上の国と地域で約9万人が活動するIQVIAの日本法人として、IQVIAジャパンでは約6,000人が一丸となり、「誰もが、より健康に自分らしく生きられる社会」の実現に向けて日々取り組んでいます。
Job OverviewAs a Project Lead in Cronos Study Operations, you will play a pivotal role in accelerating clinical trial delivery, helping bring new treatments to patients faster. You’ll be part of a core project team responsible for executing clinical studies in alignment with contractual obligations, SOPs, and global standards. This role combines strategic leadership, operational excellence, and therapeutic expertise, leveraging IQVIA’s suite of solutions to deliver high-quality results and customer satisfaction.
Key ResponsibilitiesLead or support bid defense presentations, especially for smaller or regional studies.Manage delivery of regional clinical studies, ensuring speed, quality, and cost-efficiency.Develop integrated study management plans with cross-functional teams.Oversee execution of clinical studies, ensuring compliance with tools, training, and processes.Set and communicate objectives for project teams and assess performance.Collaborate across departments to resolve issues and achieve milestones.Monitor project progress and proactively report to internal and external stakeholders.Lead risk management and resolution planning.Ensure project quality through proactive issue identification and corrective actions.Serve as the primary contact for customers and internal business development teams.Build and lead cross-functional project teams to ensure successful delivery.Drive financial success of the project, including forecasting and revenue acceleration.Manage scope changes and implement change control processes.Capture lessons learned and apply best practices.Lead vendor management activities as needed.Champion corporate initiatives and support change management.Provide performance feedback and mentorship to team members.QualificationsBachelor’s degree in Life Sciences or related field.Minimum 5 years of relevant experience, including 1+ years in project management.Strong knowledge of clinical trial conduct and regulatory requirements (ICH GCP, local laws).Broad protocol and therapeutic area knowledge.Excellent communication and presentation skills in English.Strong problem-solving and decision-making abilities.Proven leadership and cross-functional collaboration skills.Effective planning, prioritization, and time management.High attention to detail and results-oriented mindset.Proficiency in MS Office (Word, Excel, PowerPoint).Ability to work across geographies and cultures.Solid understanding of project financials and contractual obligations.Demonstrated IQVIA core competencies: Client Focus, Collaboration, Communication, Innovation, Ownership.【勤務地】
東京 品川オフィス
【雇用形態・勤務時間・福利厚生・休日休暇】雇用形態：正社員／契約社員など勤務時間：9:00-17:00フレックス勤務：あり在宅勤務制度：あり福利厚生：法定内（社会保険制度）・法定外（IQVIA独自制度）の両面から充実した福利厚生制度あり受動喫煙対策：あり休日休暇：年次有給休暇、夏季休暇、病気休暇、特別休暇、女性特別休暇、育児介護休暇、看護休暇·など試用期間：あり（通常６か月）【給与・待遇】給与：当社規定により優遇します昇給：あり賞与：あり時間外手当：あり【選考プロセス】書類選考～３次面接【応募方法】
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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com