Global Clinical Study Leader - Drive Trials & Impact

IQVIA Inc; Madrid; On-site; EUR 70,000 - 110,000; Full time

Job summary

IQVIA is seeking a Clinical Project Manager to lead regional and global clinical studies, managing timelines, budgets and quality while partnering with sponsors and cross-functional teams. The role emphasizes patient impact and regulatory compliance within a dynamic CRO environment.

The ideal candidate will have a life sciences degree and 5+ years of clinical research experience, including study leadership and strong stakeholder management in a global setting.

Qualifications

• Bachelor’s degree in Life Sciences, Healthcare, or a related field.
• 5+ years of clinical research experience, incl. project management in CRO/pharma.
• Experience leading clinical studies or study workstreams.
• Strong knowledge of ICH-GCP and regulatory requirements.
• Proven ability to manage timelines, budgets, quality.
• Experience building sponsor relationships in a global environment.

Responsibilities

• Lead regional and global clinical studies from start-up through close-out.
• Build sponsor relationships and serve as primary project contact for exceptional customer experience.
• Lead and coordinate cross-functional teams to achieve milestones and study objectives.
• Develop and execute study management plans to support delivery.
• Manage timelines, budgets, quality, risks and operational performance.
• Support financial oversight, forecasting, change control and vendor management as applicable.
• Ensure studies comply with ICH-GCP, regulatory requirements, SOPs and contractual commitments.

Skills

Life Sciences degree

Clinical research

Study leadership

ICH-GCP knowledge

Stakeholder management

Communication

Education

Bachelor's degree in Life Sciences

Job description

IQVIA is seeking a Clinical Project Manager to lead regional and global clinical studies, managing timelines, budgets and quality while partnering with sponsors and cross-functional teams. The role emphasizes patient impact and regulatory compliance within a dynamic CRO environment.

The ideal candidate will have a life sciences degree and 5+ years of clinical research experience, including study leadership and strong stakeholder management in a global setting.