Senior Clinical Project Lead - Oncology Trials

IQVIA; Lisboa; Presencial; EUR 90 000 - 130 000; Tempo integral

Resumo da oferta

IQVIA Biotech is seeking an experienced Clinical Project Manager/Senior CPM to join a respected team focusing on oncology trials. You will lead studies, manage a cross-functional core team, and ensure delivery, quality and financial performance across regions.

The role emphasizes risk management, stakeholder communication, and strict adherence to ICH GCP regulatory standards. A minimum of 4 years CPM experience and strong English communication are required.

Qualificações

• Bachelor's degree in Life sciences or related field required.
• Minimum 4 years CPM experience with regional/global scope preferred.
• Solid understanding of clinical trial conduct and regulatory requirements (ICH GCP).
• Experience in oncology trials is highly desirable.
• Strong English communication and cross-functional collaboration skills.

Responsabilidades

• Accountable for execution of clinical studies per contract while optimizing speed, quality and cost.
• Set objectives for core project team and monitor performance.
• Lead bid defense presentations and manage smaller regional studies when needed.
• Develop integrated study management plans with cross-functional teams.
• Collaborate across functional groups to achieve milestones and resolve issues.
• Monitor progress and proactively share project information with stakeholders.
• Manage risks and contingencies and drive corrective actions.
• Serve as primary or backup project contact with customers and support business development.

Conhecimentos

Project management

English communication

Regulatory knowledge

Clinical trial conduct

Budget/financial management

Stakeholder management

Cross-functional collaboration

Risk management

Planning and time management

Leadership and mentorship

Formação académica

Bachelor's degree Life sciences

Descrição da oferta de emprego

IQVIA Biotech is seeking an experienced Clinical Project Manager/Senior CPM to join a respected team focusing on oncology trials. You will lead studies, manage a cross-functional core team, and ensure delivery, quality and financial performance across regions.

The role emphasizes risk management, stakeholder communication, and strict adherence to ICH GCP regulatory standards. A minimum of 4 years CPM experience and strong English communication are required.