Senior Clinical Trial Operations Specialist

ICON Strategic Solutions; Poland; On-site; PLN 180,000 - 240,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance

Retirement planning

Global Employee Assistance Programme

Life assurance

Job summary

ICON plc is a world-leading healthcare intelligence and clinical research organization. We are seeking a Senior Clinical Trial Associate to support management and execution of clinical trials through a range of administrative and operational tasks.

As part of the team in Poland, you will take ownership of trial management deliverables, coordinate documentation, and collaborate with cross-functional teams to ensure regulatory compliance and timely study progress.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience in a clinical trial support role with regulatory knowledge.
• Strong organizational and multitasking skills.
• Proficiency in clinical trial management systems and data management.

Responsibilities

• Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records.
• Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.
• Collaborating with cross-functional teams to support trial operations and resolve issues.
• Monitoring and tracking trial progress, including managing site communications and timely delivery of study materials.
• Building and maintaining relationships with site staff and other stakeholders to facilitate smooth trial operations.

Skills

Organization

Communication

multitasking

Education

Bachelor's degree

Tools

Clinical trial management systems

Job description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We are seeking a Senior Clinical Trial Associate to support management and execution of clinical trials through a range of administrative and operational tasks.

As part of the team in Poland, you will take ownership of trial management deliverables, coordinate documentation, and collaborate with cross-functional teams to ensure regulatory compliance and timely study progress.