Oncology Clinical Lead: Global Study Delivery & Leadership

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

Resumo da oferta

IQVIA in Portugal is seeking a Clinical Lead to oversee the clinical delivery of regional and global studies, ensuring recruitment, site performance and regulatory compliance.

The role requires a strong oncology background, 5+ years in CRO/pharma, and proven ability to lead cross-functional teams and manage study milestones, budgets and stakeholder expectations. Join a global team delivering high-quality trials with data-driven insights.

Qualificações

• Bachelor's degree in Life Sciences, Healthcare, or related field.
• Strong Oncology background.
• 5+ years in clinical research, monitoring, or operations within CRO/pharma.
• Solid understanding of ICH-GCP and regulatory requirements.
• Experience leading clinical study delivery, including recruitment and site management.
• Ability to collaborate across cross-functional teams and manage stakeholders globally.

Responsabilidades

• Lead the clinical delivery of regional and global studies with quality, timeline, and recruitment goals.
• Drive patient recruitment and site engagement strategies to meet enrolment targets.
• Partner with Project Leaders and cross-functional teams to hit milestones and resolve issues.
• Provide leadership to clinical teams, oversee resource planning and training.
• Manage clinical risks and drive proactive quality improvements throughout studies.
• Build relationships with internal and external stakeholders for alignment.
• Support budgeting, forecasting and scope-change identification.
• Contribute to continuous improvement and knowledge sharing.
• Support proposal development and bid defence activities as appropriate.

Conhecimentos

Oncology background

Clinical research experience

Leadership

Cross-functional collaboration

Formação académica

Bachelor's degree in Life Sciences, Healthcare, or related field

Descrição da oferta de emprego

IQVIA in Portugal is seeking a Clinical Lead to oversee the clinical delivery of regional and global studies, ensuring recruitment, site performance and regulatory compliance.

The role requires a strong oncology background, 5+ years in CRO/pharma, and proven ability to lead cross-functional teams and manage study milestones, budgets and stakeholder expectations. Join a global team delivering high-quality trials with data-driven insights.