Clinical Data Quality Associate
- Mexico City
- Clinical Data Management
- ICON Full Service & Corporate Support
About the role
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Clinical Data Quality Associate
JR118136
Site: Mexico
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.
Overview:
Supports the preparation and conduct of clinical trials by reviewing and verifying source data and other key study deliverables to ensure quality is maintained
The role:
• Analyzes data collection and implements corrective action.
• Collaborates with internal and external reviewers on resolution of data quality inquiries.
• Collaborates with team leaders and functional managers (FMs) to identify performance metrics for clinical staff.
• Manages the reporting and analysis of trends detected in QC processes.
• Performs QC of data entry process.
• Assists with the development of new QC methods by reviewing source documentation
• Good knowledge of medical terminology
• Good knowledge of the International Conference of Harmonization (ICH) document, Good Clinical Practice (GCP), and good documentation practices in clinical research
• Solid attention to detail and prioritization skills
• Solid written and oral communication skills
• Good ability to utilize problem solving techniques and provide solutions in QC processes
You will need:
• 2 years of relevant experience
• Associate’s degree or international equivalent
• Advanced English to write, read and speak
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.
#LI-FB1
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
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