ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Clinical Study Manager at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do
Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.
Key Responsibilities Include
Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines.
Collaborate with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of clinical studies.
Develop and manage study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans.
Lead the resolution of issues and challenges that may arise during clinical trials, employing effective problem-solving skills and communication strategies.
Ensure data integrity and quality by implementing rigorous monitoring and validation processes throughout the study lifecycle.
Your Profile
You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.
Required Qualifications And Experience
Bachelor's degree in a relevant scientific discipline or healthcare-related field
Proven experience in clinical study management, with a strong understanding of the drug development process and regulatory requirements.
Excellent project management skills, including the ability to handle multiple tasks simultaneously and prioritize effectively.
Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional