Global Study Manager: Lead Clinical Trials & Teams

ICON Strategic Solutions; Polska; On-site; PLN 180,000 - 280,000; Full time

Benefits offered by this job

Competitive salary

Health insurance

Annual leave

Career development

Global exposure

Travel opportunities

Job summary

ICON Strategic Solutions seeks a Clinical Trial Manager to oversee day-to-day trial operations and ensure high-quality outcomes across our programmes. You will lead cross-functional teams, manage timelines and budgets, and drive study deliverables with a focus on compliance.

Travel to sites and investigators is expected (approximately 25%). The role offers exposure to global trials and a strategic impact on patient outcomes.

Qualifications

• University degree in medicine, science, or equivalent combination of education & experience.
• Demonstrated ability to drive the clinical deliverables of a study.
• Subject matter expertise in the designated therapeutic area.
• Prior monitoring experience is preferred.
• Willingness to travel as required (approximately 25%)

Responsibilities

• Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
• Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
• Build and manage strong relationships with trial investigators and stakeholders.
• Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Skills

Clinical trial management

Team leadership

Stakeholder management

Regulatory compliance

Education

University degree in medicine or science

Job description

ICON Strategic Solutions seeks a Clinical Trial Manager to oversee day-to-day trial operations and ensure high-quality outcomes across our programmes. You will lead cross-functional teams, manage timelines and budgets, and drive study deliverables with a focus on compliance.

Travel to sites and investigators is expected (approximately 25%). The role offers exposure to global trials and a strategic impact on patient outcomes.