Global Clinical Operations Lead – Oncology Trials

IQVIA; Madrid; Presencial; EUR 65.000 - 95.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Clinical Operations Lead to join our sponsor-dedicated Clinical FSP team. Based in Madrid, you will support trial execution, maintain timelines, and liaise with CROs and vendors to ensure on-time delivery.

The role requires strong communication across internal teams, sites, and vendors, with experience in oncology trials and ICH GCP compliance. This full-time position focuses on efficient trial operations in a global setting.

Formación

• Minimum 3 years’ experience in biopharmaceutical clinical research.
• Proven track record in clinical project management within oncology.
• Experience managing vendors and CRO relationships.
• Working knowledge of ICH GCP and regulatory requirements.
• Experience in multinational/global clinical trials is preferred.

Responsabilidades

• Assist in development and execution of trial documents and manuals.
• Create master ICF templates and update amendments.
• Support feasibility and site evaluation activities.
• Contribute to study timelines, recruitment tools, and retention plans.
• Organize team meetings with investigators and coordinators.
• Assist IP and co-medication strategy development.
• Monitor timelines and vendor deliverables (Monitoring, Sample management, IVRS, Lab).
• Build relationships with investigational sites to enhance trial conduct.
• Serve as preliminary liaison to study sites and escalate appropriately.

Conocimientos

Clinical Project Management

Oncology experience

Vendor management

ICH GCP knowledge

Multinational/global trials

Strong communication

Biopharmaceutical industry

Educación

Bachelor’s Degree in Science

Herramientas

IVRS

Laboratory coordination

Descripción del empleo

IQVIA is seeking a Clinical Operations Lead to join our sponsor-dedicated Clinical FSP team. Based in Madrid, you will support trial execution, maintain timelines, and liaise with CROs and vendors to ensure on-time delivery.

The role requires strong communication across internal teams, sites, and vendors, with experience in oncology trials and ICH GCP compliance. This full-time position focuses on efficient trial operations in a global setting.