Senior Clinical Trial Associate — Trial Operations & Compliance

ICON Clinical Research; Polska; Hybrid; PLN 180.000 - 240.000; Vollzeit

Zusammenfassung

ICON Plc, a sponsor-dedicated leader, is seeking a Senior Clinical Trial Associate to support the management and execution of clinical trials with a range of administrative and operational tasks. You will take ownership of trial deliverables, assist with regulatory documents, coordinate meetings, and work with cross-functional teams to ensure compliant, timely study progress.

The role requires strong organization, attention to detail, and up to 10% travel to sites as needed.

Qualifikationen

• Bachelor's degree in a relevant scientific discipline or healthcare field.
• Extensive experience in a clinical trial support role with regulatory knowledge.
• Strong organizational and multitasking abilities for multiple tasks and projects.
• Proficiency in CTMS and trial documentation, data management, and related software.
• Excellent communication and teamwork with diverse stakeholders.
• Willingness to travel about 10%

Aufgaben

• Provide administrative support for clinical trials, manage documentation and trial records.
• Assist in regulatory document preparation and submission per study protocols.
• Collaborate with cross-functional teams to support trial operations and issue resolution.
• Monitor trial progress and site communications, ensuring timely study material delivery.
• Build relationships with site staff and stakeholders to facilitate operations.

Kenntnisse

Clinical trial management

Regulatory compliance

Documentation

Cross-functional collaboration

Ausbildung

Bachelor's degree in relevant field

Tools

CTMS

Clinical trial software

Jobbeschreibung

ICON Plc, a sponsor-dedicated leader, is seeking a Senior Clinical Trial Associate to support the management and execution of clinical trials with a range of administrative and operational tasks. You will take ownership of trial deliverables, assist with regulatory documents, coordinate meetings, and work with cross-functional teams to ensure compliant, timely study progress.

The role requires strong organization, attention to detail, and up to 10% travel to sites as needed.