Global Clinical Trial Manager II — Study Delivery Leader

ICON Clinical Research; Poland; Hybrid; PLN 180,000 - 240,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

LifeWorks EAP

Life assurance

Flexible benefits

Job summary

ICON plc is seeking a Clinical Trial Manager II to lead and optimize multinational trials across Bulgaria, Romania, Poland, Spain, Czech Republic and Hungary. You will design, monitor and analyze trials, ensuring adherence to ICH/GCP and regulatory standards while coordinating with global teams.

Responsibilities include managing enrollment, study activity plans, TMF quality, budgets, and vendor oversight, with travel up to ~25% as required.

Qualifications

• Bachelor's degree in life sciences or related discipline.
• 5+ years of relevant study management experience in pharmaceutical/scientific environment.
• Strong project management skills and tools.
• In-depth knowledge of GCPs and ICH guidelines.
• Experience across multiple study designs and cross-functional teams.
• Leadership and ability to empower others to meet objectives.
• Excellent communication and interpersonal skills across global teams.

Responsibilities

• Oversee clinical trial management workstreams and ensure quality and timelines.
• Collaborate with cross-functional teams to design and implement trial protocols.
• Manage day-to-day operations of trials and ensure regulatory compliance.
• Analyze trial data, identify trends, and provide insights to optimize outcomes.
• Address challenges and implement solutions for trial execution.
• Communicate with stakeholders to foster partnerships and smooth processes.
• Manage study deliverables and budgets within defined plans.

Skills

Project management

Leadership

Communication

Detail orientation

Multinational collaboration

Problem solving

Education

Bachelor's degree in life sciences

Job description

ICON plc is seeking a Clinical Trial Manager II to lead and optimize multinational trials across Bulgaria, Romania, Poland, Spain, Czech Republic and Hungary. You will design, monitor and analyze trials, ensuring adherence to ICH/GCP and regulatory standards while coordinating with global teams.

Responsibilities include managing enrollment, study activity plans, TMF quality, budgets, and vendor oversight, with travel up to ~25% as required.