Senior Phase I Clinical Trial Manager – Global Ops

ICON Strategic Solutions; United States; On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Competitive retirement planning

LifeWorks Global Employee Assistance

Life assurance

Childcare vouchers

Job summary

ICON Strategic Solutions in the United States is seeking a Clinical Trial Manager to oversee day-to-day trial management within a sponsor-dedicated model. You will support your team and stakeholders to deliver high-quality outcomes across clinical programmes.

You will manage end-to-end trial activities, ensure timelines, budgets, and quality standards, and collaborate with cross-functional teams to implement protocols. Travel may be required for Phase I studies.

Qualifications

• University degree in medicine, science, or equivalent combination of education & experience.
• A minimum of three years of industry clinical trial management experience.
• Demonstrated ability to drive the clinical deliverables of a study.
• Experience managing phase I (healthy volunteer) studies.
• Some travel may be required.

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.

Education

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

Job description

ICON Strategic Solutions in the United States is seeking a Clinical Trial Manager to oversee day-to-day trial management within a sponsor-dedicated model. You will support your team and stakeholders to deliver high-quality outcomes across clinical programmes.

You will manage end-to-end trial activities, ensure timelines, budgets, and quality standards, and collaborate with cross-functional teams to implement protocols. Travel may be required for Phase I studies.