SSO Associate Clinical Project Manager

Job Description Summary

Play a pivotal role at the heart of clinical trial delivery, where your work directly supports the timely and high-quality development of innovative medicines for patients. As an SSO Associate Clinical Project Manager, you will lead country-level execution of clinical studies from initiation through close-out, working closely with cross-functional and global teams. This role offers a unique opportunity to build strong project management expertise, collaborate in a global matrix environment, and make a tangible impact on how clinical trials are delivered every day.

Job Description

Key Responsibilities

• 担当国における臨床試験の計画から実行、クローズアウトまでを一貫してリードする Lead end-to-end execution of assigned clinical studies at the country level
• グローバルおよび国内の関係者と連携し、試験の進捗・課題・リスクを適切に管理する Collaborate with global and local stakeholders to manage study progress, risks, and issues
• 試験スケジュール、進捗、KPIを管理し、品質と納期の両立を確保する Manage timelines, progress, and key performance indicators to ensure quality and delivery
• 施設およびClinical ResearchAssociateと連携し、被験者組み入れ目標の達成を推進する Drive patient recruitment performance in collaboration with sites and Clinical Research Associates
• データ品質および規制遵守を確保し、GCPおよび社内基準に沿った試験運営を行う Ensure data quality and regulatory compliance aligned with Good Clinical Practice and internal standards
• モニタリング結果をレビューし、課題の是正およびエスカレーションを適切に実施する Review monitoring outputs and drive timely issue resolution and escalation
• 監査・査察対応および継続的改善活動を通じて、試験運営の質向上に貢献する Support audit readiness and continuous improvement initiatives to enhance trial execution

Essential Requirements

• 科学系またはヘルスサイエンス分野の学士号を有していること Bachelor’s degree in a scientific or health-related discipline
• 臨床試験における実務経験を3年以上有し、モニタリングまたは試験管理に携わった経験があること At least three years of experience in clinical research, including trial oversight or monitoring
• 臨床医薬品開発プロセス全般への理解を有し、試験運営に関する知識を備えていること Solid understanding of the clinical drug development process and study execution
• グローバルかつマトリクス型の環境で協働できる能力 Ability to work effectively in a global matrix environment
• 国際的な臨床試験基準および規制要件への理解 Knowledge of international clinical trial standards and regulatory requirements
• 英語での円滑なコミュニケーション能力（読み書き・会話） Fluency in written and spoken English

Desirable Requirements

• 臨床試験におけるプロジェクトマネジメントまたはStudyLead経験 Experience in clinical trial project management or study leadership
• 多国間試験やグローバルチームとの協働経験 Experience working with global or multinational study teams

Benefits and Rewards

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Commitment to Diversity and Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Accessibility and Accommodation

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Additional Information

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Skills Desired