Clinical Associate - CTA
ICON 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 a CTA 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 data accuracy, integrity, and compliance.
Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites.
Willingness to travel as needed
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here
Are you a current ICON Employee? Please click here to apply
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.
We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
