Clinical Data Analyst

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.

Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.

Role summary

We are looking to recruit an Clinical Data Analyst as part of a specialist team responsible for building derived data libraries, Data Quality Assessment (DQA) and Key Risk Indicator (KRI) dashboards in the central monitoring platform CluePoints.com, as well as performing KRI and DQA analysis in the platform to support central monitoring.

The candidate will be working with stakeholders to define study level Risk-Rased Monitoring (RBM) strategies, hands-on deployment, processing and maintenance of data for analysis and process documentation. This position will also be expected to conduct central monitoring activities, such as system output review, signal reporting and action management. Mentorship of junior technical staff is expected and the ability to work both independently and in a matrix team environment is essential.

*This role can be based in Dublin, Paris or Warsaw (office or home based)

Key responsibilities:

*Develop and maintain study set-up in the central monitoring platform

*Define and build KRIs, ensuring standard deployment consistency and alignment with corporate standards and regulatory requirements

*Build and maintain study specific DQA dashboard, analyse and report any data quality outliers and atypicality

*Influence and communicate with key stakeholders and provide data reporting support to study teams across the research and business units

*Build and maintain collaborative working relationships with stakeholders to review reported findings, actions resolution and solve problems as and when they arise.

*Provide technical oversight, guidance and coordination for all the central monitor activities

*Implement and maintain quality control (QC) documentation for RBM activities, in accordance with departmental procedures

Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.