Clinical Trial Associate - On-Site in Warsaw

ICON Strategic Solutions; Województwo mazowieckie; In loco; PLN 80.000 - 120.000; Tempo pieno

Vantaggi offerti da questo lavoro

Health insurance

Annual leave entitlements

Retirement planning

Employee Assistance Programme

Descrizione del lavoro

ICON Strategic Solutions is seeking a Clinical Trial Associate to work on-site at the Client’s Warsaw office in Poland. The role focuses on assisting with the design and analysis of clinical trials, interpreting medical data, and contributing to the advancement of therapies.

This is a local CTA position requiring full-time presence in Warsaw. You will coordinate trials, maintain essential documents, prepare trial materials, and support cross-functional teams to ensure timely trial execution and

Competenze

• Bachelor's degree in a scientific or healthcare-related field.
• At least one year of CTA or Study Coordinator experience.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.

Mansioni

• Coordinate and administer clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintain and organize trial documentation, including study files and regulatory submissions.
• Assist in preparing study-related materials such as informed consent forms and case report forms.
• Collaborate with cross-functional teams to ensure smooth trial execution and clear communication.
• Track and report clinical trial metrics and milestones.

Conoscenze

Clinical research experience

Organizational skills

Communication skills

Team collaboration

Formazione

Bachelor's degree in a scientific or healthcare-related field

Descrizione del lavoro

ICON Strategic Solutions is seeking a Clinical Trial Associate to work on-site at the Client’s Warsaw office in Poland. The role focuses on assisting with the design and analysis of clinical trials, interpreting medical data, and contributing to the advancement of therapies.

This is a local CTA position requiring full-time presence in Warsaw. You will coordinate trials, maintain essential documents, prepare trial materials, and support cross-functional teams to ensure timely trial execution and