Global Clinical Study Manager - Sponsor-Dedicated Trials

ICON San Antonio; Center Square (PA); On-site; USD 100,000 - 140,000; Full time

Benefits offered by this job

Health insurance

Annual leave

Retirement planning

Job summary

ICON Strategic Solutions seeks a qualified Project Manager to lead global clinical studies as an FSP Clinical Study Manager. You will coordinate trial activities, manage budgets, timelines, and vendor relationships to deliver trials on time and to quality standards.

You will collaborate with global trial leaders, regulatory affairs, and CROs, ensuring inspections readiness and ongoing governance. Fluent business English and PMP/PRINCE2 are advantageous; travel is minimal.

Qualifications

• Proven track record of delivering clinical projects on time and within scope.
• Experience coordinating CRO/vendor oversight and budgeting.
• Knowledge of US CFR, ICH GCP, and global regulatory requirements.

Responsibilities

• Lead and coordinate trial activities across global studies.
• Oversee CRO/vendor selection, budgets, and performance.
• Ensure inspections readiness and regulatory compliance.

Skills

Leadership

Vendor oversight

Global regulatory knowledge

Communication

English proficiency

PMP

PRINCE2

CTMS familiarity

Budget management

Education

Bachelor's degree in life sciences

Tools

CTMS

Microsoft Project

Job description

ICON Strategic Solutions seeks a qualified Project Manager to lead global clinical studies as an FSP Clinical Study Manager. You will coordinate trial activities, manage budgets, timelines, and vendor relationships to deliver trials on time and to quality standards.

You will collaborate with global trial leaders, regulatory affairs, and CROs, ensuring inspections readiness and ongoing governance. Fluent business English and PMP/PRINCE2 are advantageous; travel is minimal.