Global Clinical Study Lead — Hybrid, Poland

POL - 6999 Takeda SCE; Warszawa; Hybrid; PLN 350,000 - 600,000; Full time

Benefits offered by this job

Hybrid work model

Equal opportunity employer

Job summary

Takeda Pharmaceutical Co. in Warsaw, Poland, is seeking an Associate Director, Clinical Study Management to lead complex, global clinical studies from planning through closeout in a hybrid work model.

You will provide independent operational leadership for study execution, drive risk management, and ensure alignment with timelines, budgets, and quality standards across internal and external partners.

Qualifications

• BS/BA required in health-related, life science, or tech fields.
• 8+ years in pharma/ CRO with 5+ years in study management.
• Experience with global/international studies and multiple therapeutic areas advantageous.

Responsibilities

• Lead end-to-end study operations for global trials with SET accountability.
• Provide independent operational leadership and decision-making for study execution.
• Ensure inspection-ready, compliant execution and closeout across study lifecycle.
• Develop Clinical Operations talent through onboarding, coaching, mentoring, and career development.
• Oversee Integrated Study Timeline and budgets, forecasting external spend.

Skills

Study management

Cross-functional leadership

Risk management

Operational budgeting

ICH-GCP compliance

English proficiency

Education

BS/BA in health-related, life science, or tech fields

Advanced degree preferred (MS/PhD)

Job description

Takeda Pharmaceutical Co. in Warsaw, Poland, is seeking an Associate Director, Clinical Study Management to lead complex, global clinical studies from planning through closeout in a hybrid work model.

You will provide independent operational leadership for study execution, drive risk management, and ensure alignment with timelines, budgets, and quality standards across internal and external partners.