Global Clinical Trial Manager — Lead High-Impact Studies

ICON Strategic Solutions; Turkey; On-site; TRY 600,000 - 900,000; Full time

Benefits offered by this job

Health insurance

Annual leave entitlements

Retirement planning offerings

Global Employee Assistance Programme

Life assurance

Job summary

ICON Strategic Solutions is seeking an experienced Clinical Trial Manager to oversee day-to-day trial operations within a sponsor-dedicated model. You will manage timelines, budgets, and quality across trials, collaborating with cross-functional teams and investigators to ensure compliance and high-quality outcomes.

Ideal candidates have solid trial-management experience, therapeutic-area expertise, and willingness to travel ~25%.

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

Regulatory compliance

Vendor management

Travel readiness

Education

Science/Medicine degree

Job description

ICON Strategic Solutions is seeking an experienced Clinical Trial Manager to oversee day-to-day trial operations within a sponsor-dedicated model. You will manage timelines, budgets, and quality across trials, collaborating with cross-functional teams and investigators to ensure compliance and high-quality outcomes.

Ideal candidates have solid trial-management experience, therapeutic-area expertise, and willingness to travel ~25%.