Global Study Manager

ICON plc • Burlington, PE

2d

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 focuses on coordinating clinical trial management delivery, resolving issues, and developing team capability. The job description also describes the position as a Clinical Study Manager, contributing to the design and analysis of clinical trials and the interpretation of complex medical data to advance treatments and therapies.

The role oversees clinical study planning, execution, and monitoring; collaborates with investigators, vendors, and internal stakeholders; manages study budgets, resources, and timelines; resolves trial-related challenges; and safeguards data integrity and quality through monitoring and validation processes. Employment is contingent on having the legal right to work in the country where the role is based.

Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Proven experience in clinical study management.
• Strong understanding of the drug development process and regulatory requirements.
• Excellent project management skills, including managing multiple tasks and prioritizing effectively.
• Strong communication and interpersonal skills, with the ability to collaborate with cross-functional teams and external partners.
• Detail-oriented, with a focus on data accuracy and high-quality standards in clinical trials.
• Legal right to work in the country where the role is based.

Responsibilities

• Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines.
• Collaborate with investigators, vendors, and internal stakeholders to support successful implementation of clinical studies.
• Develop and manage study budgets, resources, and timelines, ensuring efficient resource use and adherence to study plans.
• Lead the resolution of issues and challenges arising during clinical trials using problem-solving and communication skills.
• Ensure data integrity and quality by implementing monitoring and validation processes throughout the study lifecycle.
• Develop team capability.

Benefits

• Competitive base salary and performance-related incentives.
• 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