ポジション名
Project Manager(Cronos Study Operations)
会社紹介ビジョン
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6000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 Overview
As 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. Youll 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 IQVIAs suite of solutions to deliver high-quality results and customer satisfaction.
Key Responsibilities
- Lead 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.
Qualifications
- Bachelors 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
応募方法
応募方法の詳細や連絡先
あなたのストーリーをぜひ聞かせてください
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
Required Experience:
IC
ポジション名Project Manager(Cronos Study Operations)会社紹介ビジョン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6000人が一丸...
ポジション名
Project Manager(Cronos Study Operations)
会社紹介ビジョン
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6000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 Overview
As 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. Youll 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 IQVIAs suite of solutions to deliver high-quality results and customer satisfaction.
Key Responsibilities
- Lead 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.
Qualifications
- Bachelors 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
応募方法
応募方法の詳細や連絡先
あなたのストーリーをぜひ聞かせてください
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
Required Experience:
IC
View more
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