Global Study ManagerICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.As the world’s largest provider of Functional Service Provision (FSP), ICON Strategic Solutions embeds our teams within client organisations, serving as dedicated partners to some of the world’s leading pharmaceutical.By joining our FSP program, you’ll collaborate with an award-winning biopharmaceutical leader, renowned for innovation, inclusion, and making a real difference in patients’ lives.
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As a Global Study Manager (GSM), you’ll be fully integrated into the FSPs clinical operations team, helping to deliver innovative, general clinical studies.




You’ll ensure projects are completed on time, within budget, and to the highest quality standards, working closely with both internal teams and external partners.
This is a permanent and home-based role.What you will be doing: Support the planning, setup, execution, and close-out of global clinical studies.Oversee vendors and country teams to ensure smooth study delivery.Work closely with internal teams and external partners.Help develop and update study documents (e.g., protocols, informed consent forms).Manage third-party vendors, including contracts and budgets.
Ensure all study activities comply with regulations (ICH-GCP), SOPs, and best practices.
Contribute to meetings, audits, and inspections.
Support risk management and quality assurance efforts.
Maintain accurate study documentation and ensure inspection readiness at all times.Your profile: Bachelor’s degree (preferably in life sciences or related field).At least 5 years’ e

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