Clinical Data Risk Analyst

JR120410

Clinical Data Risk Analyst

Reginal Mexico

Home Based and Office Based

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 organization: Accountability & Delivery, Collaboration, Partnership, and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touchpoint. 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.

The Role:

The CDRA role requires both an understanding of how clinical research is conducted and proficiency in data analysis techniques. For this entry-level role, successful candidates will be either life sciences graduates with experience in clinical research and a keen interest in data, or STEM graduates with a strong understanding of human behaviour.

The Clinical Risk Management team are experts on the prediction, detection, and resolution of data quality issues that could compromise the reliability of clinical trials. During the start-up phase, they use their proficiency in protocol analysis and data review planning to support the team in the identification of potential risks to the trial. Once the study gets underway, they continuously review the data as it comes in to detect new issues as they arise. Through this adaptive approach, the CRM team reduces the time to detection for major issues and lowers the probability of losing critical trial data.

The Clinical Data Risk Analysts are functional team leads within the Clinical Data Science group, charged with reviewing the study data as it comes in to identify data quality issues and assigning them to the appropriate member of the study team for resolution.

Senior members of the team also act as SMEs for core RBQM topics such as Quality Tolerance Limits and Central Monitoring data platforms (JReview, ICONIK, Cluepoints, Medidata Studio…).

Core Responsibilities:

• Using high level knowledge of the protocol, identifies critical data and processes from protocol review, and supports protocol risk evaluation process.
• Applies in-depth knowledge of risk-based quality monitoring to guide study team through relevant processes
• Uses analytic platform to navigate through large volumes of data and identify issues
• Aggregates and summarizes data for study team
• Creates data visualizations to explain issues to sponsor
• Logs and assigns findings for data issues in the Clinical Trial Management System

What you need:

• Degree in Health Science, Computer Science, Engineering, Statistics, or equivalent
• 3-4 years of experience with Clinical Data
• Clinical Trial Experience
• Advanced English proficiency for speak/read/write
• Advanced Microsoft Excel skills

What would set you apart:

• Experience with relational databases: SQL
• Exp with clinical data systems: EDC / ePRO / CTMS / IVRS
• Experience with analytic programming languages: R, Python
• Experience with analytic software platforms: JReview, Tableau, Spotfire
• Data Visualization experience

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.

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