Global Clinical Trial Manager | Lead High-Impact Trials

ICON plc; Santiago; On-site; CLP 26,000,000 - 42,000,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings for you and

Competitive retirement planning

Global Employee Assistance Programme (

Life assurance

Country-specific optional benefits

Job summary

ICON Strategic Solutions is seeking a Clinical Trial Manager to oversee day-to-day trial management activities, supporting your team and stakeholders to deliver high-quality outcomes across our programmes.

You will manage timelines, budgets, and risk, collaborate with cross-functional teams to implement protocols, and ensure compliance with local, national, and international regulations and ethical guidelines. Travel approx. 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

Study deliverables

Travel readiness

Education

University degree in medicine, science, or equivalent combination of education & experience

Job description

ICON Strategic Solutions is seeking a Clinical Trial Manager to oversee day-to-day trial management activities, supporting your team and stakeholders to deliver high-quality outcomes across our programmes.

You will manage timelines, budgets, and risk, collaborate with cross-functional teams to implement protocols, and ensure compliance with local, national, and international regulations and ethical guidelines. Travel approx. 25%.