Global Clinical Study Manager

BeOne Medicines

. Accountable for global study delivery within agreed timelines and budget with appropriate inspection readiness quality .

Posted 11/11/2026full-timeRemote • Italy, France, SpainMid-LevelSenior💰 €63,900 - €92,600 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing global clinical studies, ensuring compliance with regulatory standards, and leading cross-functional teams to achieve study objectives within budget and timelines. Proficient in clinical operations methodologies and project management, with a focus on quality metrics and risk management.

Highest-signal resume keywords

Global Clinical Study ManagementProject Management ExperienceClinical Operations MethodologiesOncology ExperienceClinical Trial Management Systems

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ProcessesStudy Budget ManagementRisk-Based Quality ManagementStudy Document PreparationSite Selection and ActivationFeasibility AssessmentData Cleaning TimelinesPerformance FeedbackInspection ReadinessAudit Management

Soft Skills

LeadershipCollaborationCommunicationProblem-SolvingTeam Management

Tools & Technologies

MS OfficeProject Planning ApplicationsClinical Trial Management Systems

Industry Keywords

BiotechPharmaCROICH/GCPSOPsClinical ResearchStudy Vendor ManagementTrial Master FilesRegulatory SubmissionsCorrective/Preventive Actions

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Accountable for global study delivery within agreed timelines and budget with appropriate inspection readiness quality
Lead all aspects of assigned clinical studies
Lead global cross-functional study teams, including oversight of external partners, and act as point of escalation
Align study goals with clinical operations and corporate goals and objectives
Lead external vendor management and collaborate with regional subject matter experts
Provide regular study progress updates to senior management
Lead planning and management from feasibility through closeout
Manage study timelines, feasibility, trial allocation, site selection, startup, and site activation
Ensure timely availability and quality of study documents for regulatory and ethics submissions
Create, maintain, and implement study plans, systems, tools, training records, and Trial Master Files
Implement risk-based quality management processes and support data cleaning timelines
Plan and execute Clinical Study Reports with Medical Writing and study team members
Monitor compliance with protocol, SOPs, ICH/GCP, study plans, and regulations
Manage quality metrics, inspection readiness, audits, inspections, risks, and corrective/preventive actions
Develop and share best practices and contribute to SOP and work-instruction improvements
Select and manage study vendors and approve invoice payments
Manage study budgets, forecasts, accruals, resources, and contingency plans
Ensure studies are executed within approved timelines, quality, and cost parameters
Provide performance feedback on team members as required

Requirements

What you’ll need

Bachelor’s Degree in a scientific or healthcare discipline required; higher degree preferred
Exceptions might be made for candidates with relevant clinical operations experience
Proven project management experience in global clinical studies; oncology experience preferred
Advanced knowledge of clinical operations methodologies and in-depth understanding of clinical study processes
Able to independently lead global clinical studies; pivotal study management experience required
5+ years of progressive experience in clinical research within biotech, pharma, or CRO industry
Proficiency with MS Office, project planning applications, and clinical trial management systems
Travel might be required as per business need

Benefits

Comp & perks

Equal opportunity employment
Travel as required by business need