Clinical Data Risk Analyst

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

With our patients at the center 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.

We have an incredible opportunity for a Clinical Data Risk Analyst to join ICON’s Clinical Data Science team.

LOCATION: home-based or office-based

• Mexico
• Colombia

OVERVIEW OF THE ROLE:

The Clinical Data Risk Analyst (CDRA) is the Clinical Risk Management and Central Monitoring Functional Lead. They are responsible for clinical data analysis components of clinical studies, including RBQM facilitation, planning, selection of KRIs focusing on identified risks, advanced analytics design and programming specifications, review of centrally aggregated data to identify risk and issues impacting data integrity, patient safety, regulatory compliance. The CDRA is responsible for signal tracking, system user support, and communication of trends to internal and external stakeholders.
 

TO BE SUCCESSFUL, YOU WILL NEED:

• 3+ years of clinical research experience (either in pharmaceutical, biotech, or CRO organization)
• Enhanced functional knowledge of Central Monitoring and supporting data platforms
• An aptitude for understanding analytic modelling methods such as regression, classification, and clustering
• Ability to effectively navigate through large volumes of data and interpret data problems
• Strong skills in aggregate data review and interpretation using visualization/analysis software (i.e. CluePoints, Medidata, DETEC, Saama, SAS, Tableau, JMP)
• Ability to read and understand a Clinical Trial Protocol
• Strong communication skills
• Strong multitasking skills
• Bachelor’s degree
   

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.

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