Global Study Associate Director - Single Sponsor Dedicated (Clinical Research)

Location: Warsaw, Poland

Salary: 225,500–418,600 PLN annualized base pay

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Lead cross-functional clinical study teams and provide direction throughout the study lifecycle.
• Coordinate communication among internal functions, external partners, service providers, and the Clinical Program Team.
• Oversee study plans, milestones, KPIs, quality standards, risk management, issue escalation, and corrective action plans.
• Manage CROs and other study-level vendors, ensuring delivery against contracted goals, timelines, budgets, and quality requirements.
• Oversee essential study documentation, Trial Master File completion, quality control, governance compliance, and inspection readiness.
• Manage budget re-forecasting, financial risks, progress reporting, and study change control.

Requirements

• University degree or equivalent, preferably in medical or biological sciences or a clinical research-related discipline.
• At least 5 years of relevant clinical experience in the pharmaceutical industry, including 2 years of project management experience, or an equivalent combination of education, training, and experience.
• Extensive knowledge of ICH-GCP, clinical research regulations, clinical study management, and clinical or drug development.
• Strong project management, team leadership, communication, conflict management, strategic thinking, organizational, and problem-solving skills.
• Ability to manage competing priorities and maintain effective relationships with internal and external stakeholders.

Culture & Benefits

• Full-time employment with a potential annualized base pay range of 225,500–418,600 PLN.
• Potential incentive plans, bonuses, health and welfare benefits, and other compensation may be available depending on the position.
• Opportunities to mentor less experienced colleagues and support professional development.
• Participation in process improvement initiatives and work as a subject matter expert for Study Management processes or systems.