Associate Clinical Project Manager

Novartis

. Lead end-to-end execution of assigned clinical studies at the country level .

Posted 11/11/2026full-timeToranomon • JapanMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical studies, ensuring compliance with Good Clinical Practice, and driving patient recruitment performance. Proficient in clinical trial project management and collaboration within global study teams.

Highest-signal resume keywords

Clinical Research ExperienceTrial OversightRegulatory ComplianceProject ManagementStakeholder Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ExecutionData Quality ManagementKey Performance IndicatorsPatient RecruitmentClinical Drug Development Process

Soft Skills

Effective CommunicationProblem SolvingCollaboration

Industry Keywords

Good Clinical PracticeInternational Clinical Trial StandardsAudit ReadinessContinuous ImprovementGlobal Matrix Environment

About the role

Key responsibilities & impact

Lead end-to-end execution of assigned clinical studies at the country level
Collaborate with global and local stakeholders to manage study progress, risks, and issues
Manage timelines, progress, and key performance indicators to ensure quality and delivery
Drive patient recruitment performance in collaboration with sites and Clinical Research Associates
Ensure data quality and regulatory compliance aligned with Good Clinical Practice and internal standards
Review monitoring outputs and drive timely issue resolution and escalation
Support audit readiness and continuous improvement initiatives to enhance trial execution

Requirements

What you’ll need

Bachelor’s degree in a scientific or health-related discipline
At least three years of experience in clinical research, including trial oversight or monitoring
Solid understanding of the clinical drug development process and study execution
Ability to work effectively in a global matrix environment
Knowledge of international clinical trial standards and regulatory requirements
Fluency in written and spoken English
Experience in clinical trial project management or study leadership
Experience working with global or multinational study teams