Clinical Trial Associate: Study Design & Global Trials

ICON Clinical Research; Polska; Hybrid; PLN 120,000 - 180,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance options for you and/或

Retirement planning

LifeWorks EAP program

Life assurance

Country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Clinical Trial Associate to join a sponsor-dedicated team. You will assist with design and analysis of trials, interpret complex medical data, and contribute to advancing treatments and therapies.

Key responsibilities include supporting day-to-day study activities, regulatory readiness, and collaboration with study teams and CROs. A background in clinical research with Veeva experience and strong communication is required.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• 1-2 years' experience in pharmaceutical industry or CRO as CTA or Study Coordinator.
• Experience in Phase 2/3 studies and global/international studies is advantageous.
• Experience using Veeva system.
• Experience across multiple therapeutic areas including oncology is advantageous.
• Knowledge of global/regional regulatory and compliance requirements for clinical research.
• Strong task management and cross-functional collaboration.
• Excellent communication, teamwork, and problem-solving skills.
• Fluent business English (oral and written).
• Willingness to travel approximately 10%.

Responsibilities

• Provide support for day-to-day clinical study activities including regulatory readiness.
• Collaborate with Clinical Operations/Study Manager, study teams and CROs to support clinical study activities as defined by the operating model.
• Perform departmental tasks as needed.

Skills

Communication skills

Teamwork

Cross-functional collaboration

Attention to detail

Willingness to travel

English proficiency

Education

Bachelor's degree

Tools

Veeva system

Job description

ICON Strategic Solutions is seeking a Clinical Trial Associate to join a sponsor-dedicated team. You will assist with design and analysis of trials, interpret complex medical data, and contribute to advancing treatments and therapies.

Key responsibilities include supporting day-to-day study activities, regulatory readiness, and collaboration with study teams and CROs. A background in clinical research with Veeva experience and strong communication is required.