Clinical Data Analyst

Company:
Location: Dublin, County Dublin

*** Mention DataYoshi when applying ***

Job Advert Posting

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

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-Based 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.

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 knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, 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.

*** Mention DataYoshi when applying ***

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