Global Study Manager - Single Sponsor dedicated (in EMEA)

IQVIA seeks a Global Study Manager to support clinical study delivery across EMEA and Africa, working with study directors on protocol development, site coordination, and regulatory compliance. The role involves cross-functional collaboration with internal teams and external partners, document management, budget oversight, and ensuring adherence to ICH/GCP guidelines throughout the study lifecycle. Candidates should hold a relevant degree and possess 3+ years of pharmaceutical or clinical research experience.

Responsibilities

• Lead preparation of delegated study documents including informed consent forms and clinical study agreements
• Maintain interactions with internal functions and external partners including CROs for efficient study delivery
• Ensure investigational product supply and study materials availability through clinical supply chain coordination
• Identify risks and issues proactively, developing mitigation and action plans for study continuity
• Verify completeness and quality of study documents in Trial Master File and support budget management activities

Requirements

• University degree in medical, biological sciences, or clinical research discipline
• At least 3 years pharmaceutical industry or academic clinical research experience
• Knowledge of clinical development process across multiple phases and therapy areas
• Expert-level understanding of ICH/GCP international guidelines
• Advanced computer skills and excellent English communication abilities
• Project management capabilities with demonstrated collaborative and independent work
• Leadership skills and external service provider management experience

Compensation: 171,500.00 zł - 404,600.00 zł base annual salary