ICON plc
Contract Research Organizations (CRO)
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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 Clinical Associate you would be an integral part of the study team whilst acquiring clinical and corporate knowledge of clinical trial conduct.
What you will do:
Provide administrative support to the Project Manager(s), Clinical Trial Manager(s) and/or sites, with emphasis on driving global inspection readiness. Clinical Associate main responsibilities will be tracking and maintenance of study activities. Responsible for the maintenance of the Trial Master File (TMF) throughout the study.
You will need:
Bachelorβs degree preferred in a scientific/medical discipline or equivalent experience.
An understanding of Pharmaceutical industry process with previous exposure to medical terminology and GCPs is preferred.
Familiarity with Windows-based computer applications (e.g., MS Excel and PowerPoint).
You will possess good written and verbal communication in English
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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.
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