Global Study Lead — Clinical Ops & Delivery

Iqvia; Madrid; On-site; EUR 39,000 - 92,000; Full time

Job summary

IQVIA in Madrid is seeking a Global Study Manager to support delivery of clinical studies from CSP development through CSR and archiving. You will work with internal and external partners to ensure on-time, on-budget, high-quality study execution.

Essential skills include leading study documents, risk mitigation, budget support, and strong English communication. The role requires collaboration and leadership across cross-functional teams.

Qualifications

• University degree in medical or biological sciences or related discipline.
• At least 3 years’ experience in pharmaceutical industry or equivalent.
• Knowledge of clinical development process and ICH/GCP guidelines.
• Excellent verbal and written English communication.

Responsibilities

• Lead preparation of delegated study documents (e.g., ICF, master Clinical Study Agreement).
• Maintain interactions with CROs and external providers to ensure timely, cost-effective, quality study delivery.
• Plan and conduct internal/external meetings (Investigators’/Monitors’ meetings).
• Coordinate supply of investigational product with Clinical Supply Chain or providers.
• Contribute to risk identification and mitigation plans.
• Ensure study documents are complete and Quality-verified in Trial Master File.
• Support budget management with GSD/GSAD, including invoicing reconciliation.
• Adhere to global processes and ICH/GCP; ensure inspection readiness.
• Support project management activities per delegation; oversee CROs during outsourced studies.
• Take on non-drug project work for process improvements as agreed.

Skills

Clinical development

ICH/GCP knowledge

Project management

Communication skills

Leadership

English fluency

Collaboration

Independent work

Computer proficiency

Education

University degree in medical/biological sciences

Job description

IQVIA in Madrid is seeking a Global Study Manager to support delivery of clinical studies from CSP development through CSR and archiving. You will work with internal and external partners to ensure on-time, on-budget, high-quality study execution.

Essential skills include leading study documents, risk mitigation, budget support, and strong English communication. The role requires collaboration and leadership across cross-functional teams.