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 UK home-based In Vitro Diagnostics CRA at ICON, you will contribute to our clinical trial operations function, working in an enthusiastic, dynamic team.
This is a unique opportunity to move from a lab-based setting into a CRA role, embedded into a blue chip clinical diagnostics project, you will join your colleagues in leading the design, planning, co-ordinating and conducting of all activities involved in initiating, monitoring and completing clinical research studies for in vitro diagnostics.
Responsibilities:
Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders. Key responsibilities include:
Your Profile:
You will bring relevant In Vitro Diagnostics experience, ideally from a laboratory background, along with the following qualifications and skills. Required qualifications and experience:
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.
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.