Senior Clinical Data Coordinator

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.

We have an incredible opportunity for a Senior Clinical Data Coordinator (CDC) to join the team.

Location Options:

• Mexico City (office-based 2-3 days/week - once the office reopens)
• United States (office-based or home-based)
• Canada (office-based or home-based)

Summary

As a Senior Clinical Data Coordinator at ICON, you will work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified Clinical Data Managers to identify, select, initiate and closeout investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.

Highlights of Key Responsibilities:

• Review CRF I eCRF data for completeness, accuracy, and consistency via computerize edits and manual data checks.
• Perform external data reconciliation and SAE reconciliation
• Generate and close/resolve (as appropriate) data queries
• Freeze and/or lock eCRFs (as appropriate) within the Electronic Data Capture System
• Create and maintain study files and other appropriate study documentation
• Perform User Acceptance Testing (UAT) and collaboratively work with CDMS personnel to see issues found through re-testing and resolution
• Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures
• Train and guide less experienced CDCs in data management requirements and activities.
  

Requirements:

• 2+ years of clinical research industry experience, within a data management role
• Prior experience performing data management duties such as reviewing CRF data, performing UAT, resolving queries etc.
• Excellent written and oral communication skills
• Excellent accuracy and attentiveness to detail
• Knowledge of database technologies and processes
• Knowledge of regulatory guidelines in relation to data quality and clinical trials conduct
• Bachelors degree in a scientific discipline

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.