Clinical Data Risk Analyst

JR120410

Clinical Data Risk Analyst

Reginal Mexico

Home 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:

Clinical risk management and central monitoring functional lead

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.

Responsible for signal tracking, system user support, communication of trends to internal and external stakeholders.

Responsibilities:

• Enhanced functional knowledge of Central Monitoring and supporting data platforms

Using high level  knowledge of the protocol, identifies critical data and processes from protocol review, and supports protocol risk evaluation process.

Aptitude for understanding analytic modeling methods such as regression, classification and clustering.

            Skill to efficiently navigate through large volumes of data and interpret data problems

Skill in aggregate data review and interpretation using visualization/ analysis software

Business Expertise:

• Ability to apply enhanced knowledge of Central Monitoring to clinical studies.

What you need:

• Degree in Pharmacy or Science, or equivalent
• 3-4 years of exp. with Clinical Data
• Clinical Trial Experience
• Advanced English for write / read an speak
• Exp with analytical systems: EDC / RDC / SQL (desirable)
• Excel Experience
• Power BI Experience
• Programming language exp.

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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