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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing complex oncology clinical trials, ensuring compliance with ICH-GCP and regulatory requirements, while providing leadership and direction to cross-functional teams. Proficient in project management methodologies and clinical study lifecycle management to enhance operational performance and efficiency.
Highest-signal resume keywords
Clinical Trial ManagementOncology Clinical TrialsICH-GCP ComplianceProject CoordinationStakeholder Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ResearchStudy OperationsSite OversightVendor Relationship ManagementPatient Recruitment StrategiesData Cleaning ActivitiesQuality Standards OversightResource Utilization MonitoringProject Planning ToolsStudy Management Processes
Soft Skills
LeadershipCommunicationOrganizationNegotiationProblem-Solving
Tools & Technologies
Clinical Trial SystemsTrial Planning Tools
Industry Keywords
PharmaceuticalHealthcare OrganizationContract Research OrganizationSOPsClinical Trial Processes
About the role
Key responsibilities & impact- Lead end-to-end performance and project management of assigned clinical trial protocols
- Manage study start-up activities, including site selection strategies, monitoring plans, and trial planning tools
- Review and contribute to patient recruitment and retention strategies
- Provide leadership, guidance, and direction to project team members across multiple locations and functions
- Evaluate project resource requirements and monitor resource utilization throughout the study lifecycle
- Address and resolve site issues, escalating risks and ensuring timely closure
- Monitor study timelines, patient recruitment, retention, and data cleaning activities
- Maintain oversight of quality standards and follow up on quality-related issues
- Drive process improvements to enhance study efficiency and operational performance
- Contribute to revenue recognition forecasting and project planning activities
- Collaborate on database lock activities and study close-out deliverables
- Ensure completion of administrative close-out procedures, study archiving, and client documentation requirements
- Manage complex oncology clinical trials for a pharmaceutical client
- Ensure compliance with ICH-GCP, local regulations, client requirements, and quality standards
Requirements
What you’ll need- Degree in a life science, nursing qualification, or relevant clinical and/or clinical management experience
- Substantial experience in clinical research, including relevant experience as a team leader in clinical functions or proven experience coordinating clinical trials
- Knowledge of ICH-GCP, regulatory requirements, SOPs, and clinical trial processes
- Experience managing clinical trial activities, study operations, site oversight, and vendor relationships
- Strong leadership, stakeholder management, and project coordination skills
- Ability to collaborate across cross-functional and global teams
- Strong communication, organization, leadership, negotiation, and problem-solving skills
- Strong command of written and spoken English
- Comfort working with clinical trial systems, study management processes, and project planning tools
- Previous experience as a Clinical Research Associate (CRA) (preferred)
- Experience in oncology clinical trials (preferred)
- Experience within a pharmaceutical company, healthcare organization, or contract research organization (preferred)
- Knowledge of project management methodologies and clinical study lifecycle management (preferred)
Benefits
Comp & perks- Medical Plan
- Life Assurance
- Pension
- Comprehensive benefits package for eligible employees
- Additional benefit offerings in accordance with the terms of applicable plans
- Home-based work capacity in France
- Leadership opportunities
- Continuous development
- Career progression opportunities