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 Senior Clinical Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency.
What You Will Do
You will lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement.
Key Responsibilities Include
Managing and coordinating clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines.
Collaborating with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies.
Overseeing site management and monitoring to ensure data integrity and compliance with study protocols.
Providing guidance and support to clinical staff and investigators,
ensuring adherence to best practices and regulatory standards.
Tracking and reporting on trial progress, identifying potential risks, and implementing strategies to mitigate challenges.
Your Profile
You will have a strong foundation in clinical coordination, with the experience to work independently and guide others.
Required Qualifications And Experience
Bachelor's degree in a relevant scientific discipline or healthcare-related field
Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.
Detail-oriented with a proactive approach to ensuring trial success and addressing clinical chall