Global Study Manager: Lead Global Clinical Trials

KCR Placement; Burlington (MA); On-site; USD 90,000 - 150,000; Full time

Job summary

ICON Strategic Solutions is seeking a Global Study Manager to lead day-to-day clinical trial management within a sponsor-dedicated model, backed by ICON’s global expertise. You will support cross-functional teams to deliver high-quality outcomes across multiple programmes.

Ideal candidates hold a university degree in medicine or science, with experience driving study deliverables, regulatory knowledge, and willingness to travel ~25%.

Qualifications

• University degree in medicine, science, or equivalent with experience.
• Ability to drive 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 protocols and procedures.
• Build and manage relationships with trial investigators and stakeholders.
• Ensure trials comply with regulations and ethical guidelines.
• Problem-solve decisions on trial design, vendor selection, and risk management.

Skills

Clinical trial management

Leadership

Regulatory compliance

Vendor management

Travel readiness

Education

Degree in medicine or science

Job description

ICON Strategic Solutions is seeking a Global Study Manager to lead day-to-day clinical trial management within a sponsor-dedicated model, backed by ICON’s global expertise. You will support cross-functional teams to deliver high-quality outcomes across multiple programmes.

Ideal candidates hold a university degree in medicine or science, with experience driving study deliverables, regulatory knowledge, and willingness to travel ~25%.