Global Clinical Trial Lead

ICON San Antonio; Center Square (PA); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Health insurance

Annual leave entitlements

Retirement planning offerings

Global Employee Assistance Programme

Job summary

ICON Strategic Solutions seeks a Clinical Trial Manager to lead day-to-day trial management within a sponsor-dedicated model, supported by ICON’s global expertise. You will support your team and stakeholders to deliver high-quality outcomes across our clinical programmes.

Key responsibilities include planning and managing trials, collaborating on protocols, building investigator relationships, and ensuring compliance with regulations and ethical guidelines. Travel approximately 25% is required.

Qualifications

• Experience leading clinical trial management efforts and delivering study deliverables.
• 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 approximately 25%

Responsibilities

• Plan and manage all aspects of clinical trials, ensuring timelines, budget, and quality.
• Collaborate with cross-functional teams to implement trial protocols and procedures.
• Build and manage relationships with trial investigators and stakeholders.
• Ensure trials comply with local, national, and international regulations and ethical guidelines.

Skills

Clinical trial management

Team development

Regulatory knowledge

Travel willingness

Monitoring experience

Education

University degree in medicine or science

Job description

ICON Strategic Solutions seeks a Clinical Trial Manager to lead day-to-day trial management within a sponsor-dedicated model, supported by ICON’s global expertise. You will support your team and stakeholders to deliver high-quality outcomes across our clinical programmes.

Key responsibilities include planning and managing trials, collaborating on protocols, building investigator relationships, and ensuring compliance with regulations and ethical guidelines. Travel approximately 25% is required.