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 Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
What You Will Do
You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.
Key Responsibilities Include
Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation.
Collaborate with cross-functional teams including Clinical Operations, Data Management,
and Biometrics to support the successful execution of clinical trials.
Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures.
Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports.
Your Profile
You will bring relevant clinical coordination experience, along with the following qualifications and skills.
Required Qualifications And Experience
Bachelor's degree in a relevant scientific discipline or healthcare-related field
Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively.
Excellent attention to detail and problem-solving abilities, with a commitment to ensuring dat