Clinical Trial Associate — Warsaw (On-Site)

KCR Placement; Warszawa; Ibrido; PLN 90.000 - 130.000; Tempo pieno

Vantaggi offerti da questo lavoro

Various annual leave entitlements

Health insurance offerings to suit you

Competitive retirement planning

Global Employee Assistance Programme

Descrizione del lavoro

ICON Strategic Solutions is seeking a Clinical Trial Associate to support the design and analysis of clinical trials from the client’s Warsaw office. You will assist with regulatory submissions, trial documentation, and cross-functional coordination to ensure high-quality trial execution.

With a bachelor’s degree in science or healthcare and at least one year of CTA/Study Coordinator experience, you will contribute to a global, sponsor-dedicated model that advances patient-centered therapies.

Competenze

• Bachelor's degree in a scientific or healthcare-related field.
• At least one year of experience as CTA or Study Coordinator.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced environment with attention to detail.
• Ability to work full time from Client's office in Warsaw.

Mansioni

• Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
• Support the preparation of study-related materials, such as informed consent forms and case report forms.
• Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
• Contribute to the tracking and reporting of clinical trial metrics and milestones.

Conoscenze

Organizational skills

Communication skills

Collaboration

Attention to detail

Formazione

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

Descrizione del lavoro

ICON Strategic Solutions is seeking a Clinical Trial Associate to support the design and analysis of clinical trials from the client’s Warsaw office. You will assist with regulatory submissions, trial documentation, and cross-functional coordination to ensure high-quality trial execution.

With a bachelor’s degree in science or healthcare and at least one year of CTA/Study Coordinator experience, you will contribute to a global, sponsor-dedicated model that advances patient-centered therapies.