Oncology Clinical Lead — Global Study Delivery

IQVIA Argentina; Madrid; Presencial; EUR 70.000 - 110.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Clinical Lead based in Madrid to oversee the clinical delivery of assigned studies, ensuring recruitment, site performance, quality, and regulatory compliance. You will collaborate with project leaders and cross-functional teams to meet milestones while guiding clinical teams and managing risks.

The role emphasizes strong oncology expertise, ICH-GCP knowledge, and experience in CRO/pharma environments, with opportunities to influence global study delivery and sponsor

Formación

• Bachelor's degree in Life Sciences, Healthcare, or a related scientific discipline.
• 5+ years of clinical research, monitoring, or clinical operations experience within a CRO, pharmaceutical, or biotechnology environment.
• Strong Oncology background with knowledge of ICH-GCP and regulatory requirements.

Responsabilidades

• Lead the clinical delivery of regional and global studies to meet quality, timeline, recruitment, and operational objectives.
• Drive patient recruitment and site engagement strategies to achieve enrolment targets.
• Partner with Project Leaders and cross-functional teams to drive milestones and maintain operational excellence.
• Provide leadership to clinical teams, supporting resource planning, training and delivery.
• Manage clinical risks and oversee quality standards with proactive mitigation.

Conocimientos

Oncology background

Clinical operations

Stakeholder management

ICH-GCP

Educación

Bachelor's degree in Life Sciences

Descripción del empleo

IQVIA is seeking a Clinical Lead based in Madrid to oversee the clinical delivery of assigned studies, ensuring recruitment, site performance, quality, and regulatory compliance. You will collaborate with project leaders and cross-functional teams to meet milestones while guiding clinical teams and managing risks.

The role emphasizes strong oncology expertise, ICH-GCP knowledge, and experience in CRO/pharma environments, with opportunities to influence global study delivery and sponsor