Clinical Study Manager II: Lead Complex Trials

ICON Clinical Research; Polska; Hybrid; PLN 184.000 - 289.000; Vollzeit

Benefits dieser Stelle

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme (

Life assurance

Country-specific benefits

Zusammenfassung

ICON Clinical Research is seeking a Laboratory Study Manager for Bulgaria to oversee day-to-day management of complex clinical trials and lead cross-functional teams. The role focuses on delivering quality outcomes and ensuring regulatory compliance while driving study plans, budgets, and timelines.

The candidate will manage complex trials, coordinate with investigators and vendors, and maintain high data integrity, supporting ICON’s global expertise and sponsor-dedicated model.

Qualifikationen

• Bachelor's degree in a relevant scientific discipline or healthcare field.
• Extensive experience in clinical study management and drug development processes.
• Proven project management with ability to handle multiple tasks and priorities.
• Exceptional communication and interpersonal skills for cross-functional collaboration.
• Detail-oriented with focus on data accuracy and high quality standards in trials.

Aufgaben

• Lead planning, execution, and monitoring of complex clinical trials ensuring regulatory compliance and timelines.
• Collaborate with investigators, vendors, and internal partners to drive advanced clinical studies.
• Develop and manage study plans, budgets, and timelines; optimize resource use.
• Lead issue resolution with strategic problem-solving and clear communication.
• Oversee monitoring/validation processes to ensure data integrity throughout the lifecycle.

Kenntnisse

Cross-functional collaboration

Regulatory awareness

Data interpretation

Team development

Ausbildung

Bachelor's degree in science/healthcare

Jobbeschreibung

ICON Clinical Research is seeking a Laboratory Study Manager for Bulgaria to oversee day-to-day management of complex clinical trials and lead cross-functional teams. The role focuses on delivering quality outcomes and ensuring regulatory compliance while driving study plans, budgets, and timelines.

The candidate will manage complex trials, coordinate with investigators and vendors, and maintain high data integrity, supporting ICON’s global expertise and sponsor-dedicated model.