Global Study Manager

ICON plc • Burlington, PE

3d

About The Position

At ICON Strategic Solutions, the Global Study Manager works in a sponsor-dedicated model, supported by ICON’s global expertise. The role manages clinical trial operations activities and supports the team and stakeholders in delivering high-quality outcomes across clinical programmes.

Requirements

• University degree in medicine, science, or an equivalent combination of education and experience.
• Demonstrated ability to drive the clinical deliverables of a study.
• Subject matter expertise in the designated therapeutic area.
• Willingness to travel as required, approximately 25%.
• Must have the legal right to work in the country where the role is based.

Nice To Haves

• Prior monitoring experience.

Responsibilities

• Manage day-to-day clinical trial management activities and support the team in delivering quality outcomes.
• 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 trials comply with local, national, and international regulations and ethical guidelines.
• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.
• Drive the clinical deliverables of a study.

Benefits

• Competitive base salary and performance-related incentives.
• Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.

What This Job Offers

• Job Type: Full-time