USA Clinical Trial Manager | Regional Lead

ICON Strategic Solutions; United States; On-site; USD 110,000 - 160,000; Full time

Benefits offered by this job

Health & wellbeing programs

Retirement plans

Life insurance

Employee assistance program

Career development opportunities

Competitive salary & incentives

Job summary

ICON Strategic Solutions is seeking a Clinical Trial Manager to oversee day-to-day management of clinical trials, ensuring timelines, budgets, and quality standards are met. You will work with cross-functional teams, investigators, and stakeholders to implement protocols, manage risks, and maintain regulatory compliance across regional and global programs.

The role requires a strong background in clinical trial management, the ability to drive deliverables, and willingness to travel up to 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 development

Regulatory compliance

Vendor management

Risk management

Travel readiness

Education

University degree in medicine or science

Job description

ICON Strategic Solutions is seeking a Clinical Trial Manager to oversee day-to-day management of clinical trials, ensuring timelines, budgets, and quality standards are met. You will work with cross-functional teams, investigators, and stakeholders to implement protocols, manage risks, and maintain regulatory compliance across regional and global programs.

The role requires a strong background in clinical trial management, the ability to drive deliverables, and willingness to travel up to 25%.