Global Clinical Study Manager - Trials Leader

KCR Placement; Reading; On-site; GBP 75,000 - 110,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance

Retirement planning

LifeWorks, EAP

Job summary

ICON Strategic Solutions is seeking a Global Study Manager to lead day-to-day clinical trial management within a sponsor-dedicated model, leveraging ICON’s global expertise to deliver high-quality outcomes across multiple programmes.

You will plan trials, collaborate across functions, manage investigator relationships, ensure regulatory compliance, and travel up to 25% to sites. The role offers career development in a supportive, inclusive environment and a competitive salary.

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

Therapeutic area expertise

Monitoring experience (preferred)

Travel willingness

Education

University degree in medicine/science or equivalent

Job description

ICON Strategic Solutions is seeking a Global Study Manager to lead day-to-day clinical trial management within a sponsor-dedicated model, leveraging ICON’s global expertise to deliver high-quality outcomes across multiple programmes.

You will plan trials, collaborate across functions, manage investigator relationships, ensure regulatory compliance, and travel up to 25% to sites. The role offers career development in a supportive, inclusive environment and a competitive salary.