Remote Clinical Trial Manager II – Poland

Syneos Health, Inc.; United States; Remote; USD 46,000 - 71,000; Full time

Job summary

Syneos Health, Inc. is seeking a Clinical Trial Manager II for a home-based role in Poland. You will oversee Phase 1 through Phase 4 clinical studies, coordinating across functions to ensure timelines, quality, and regulatory compliance while maintaining patient safety.

The ideal candidate has leadership experience in site management, risk-based monitoring, CTMS/EDC proficiency, and the ability to operate in an international environment. Some travel may be required.

Qualifications

• Bachelor’s degree or RN in a related field required.
• Demonstrated ability to lead and align teams on complex projects.
• Proven capability in international collaboration and coordination.
• Expertise in site management and monitoring (clinical or central).
• Experience with risk-based monitoring and budget management."
• Knowledge of Good Clinical Practice/ICH guidelines and regulatory requirements.
• Strong computer skills and data-driven decision making.
• Excellent conflict resolution and communication skills.
• Willingness to travel up to ~20% of time.

Responsibilities

• Lead development, coordination, and execution of Phase 1–4 clinical studies across sites.
• Collaborate with investigators, client teams, and operations to meet milestones and budgets.
• Oversee site management, monitoring deliverables, patient safety, and data integrity.
• Coordinate CTMS/EDC tool use, dashboards, and documentation.
• Provide training to study teams on protocol specifics, CRF completion, and timelines.

Skills

Leadership

International experience

Problem solving

Communication

Quality and compliance

Financial/budget awareness

Computer skills

Risk-based monitoring

Site management

CTMS/EDC proficiency

Travel readiness

Education

Bachelor’s degree or RN in a related field

Job description

Syneos Health, Inc. is seeking a Clinical Trial Manager II for a home-based role in Poland. You will oversee Phase 1 through Phase 4 clinical studies, coordinating across functions to ensure timelines, quality, and regulatory compliance while maintaining patient safety.

The ideal candidate has leadership experience in site management, risk-based monitoring, CTMS/EDC proficiency, and the ability to operate in an international environment. Some travel may be required.