Clinical Data Analyst

2 semanas atrás


São Paulo, São Paulo, Brasil ICON Tempo inteiro
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.

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.

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:


We are looking to recruit an Clinical Data Analyst as part of a specialist team responsible for building derived data libraries, Data Quality Assessment (DQA) and Key Risk Indicator (KRI) dashboards in the central monitoring platform CluePoints, as well as performing KRI and DQA analysis in the platform to support central monitoring.

**_ *This role can be based in Lithuania, Bulgaria, Czech Republic, Hungary, Romania, Latvia or Columbia
- home based or office based*_**Key responsibilities:
  • Develop and maintain study set
  • up in the central monitoring platform
  • Define and build KRIs, ensuring standard deployment consistency and alignment with corporate standards and regulatory requirements
  • Build and maintain study specific DQA dashboard, analyse and report any data quality outliers and atypicality
  • Influence and communicate with key stakeholders and provide data reporting support to study teams across the research and business units
  • Build and maintain collaborative working relationships with stakeholders to review reported findings, actions resolution and solve problems as and when they arise.
  • Provide technical oversight, guidance and coordination for all the central monitor activities
  • Implement and maintain quality control (QC) documentation for RBM activities, in accordance with departmental procedures
  • Manage own time and priorities effectively while working on multiple projects
  • Mentor and supervise less junior staff and be responsible for the quality and accuracy of the work done

Key Requirements:

  • Bachelor's degree, or equivalent level qualification in Natural Sciences, Mathematics, Computer Science, Information Management or Information Technology, or have gained experience in a similar discipline.
  • Experience in developing in _R, SAS_ or any other _SQL_ languages is desired, but not critical
  • Good understanding of data modelling and manipulation techniques, including ETL and aggregation methods
  • Project management experience and proven business analysis and requirements elicitation skills
  • Good presentation skills and proven ability communicating requirements and solutions to team members and stakeholder
  • Working knowledge of clinical development process and good understanding of clinical data management
  • Desired experience in clinical risk management, central monitoring strategies and statisticsbased data profiling

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.

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