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Senior CDC

  1. Mexico
2024-110773
  1. Clinical Data Management, Clinical Data Scientist Lead, Clinical Systems, Data Standards Consultant
  2. ICON Strategic Solutions
  3. Remote

About the role

This vacancy has now expired. Please see similar roles below...

As a Senior Clinical Data Coordinator (Sr CDC) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

 

Working within one of our newest partnerships you will be embedded in a global company that has relentlessly followed the science to find solutions for patients with critical unmet medical needs. On this top pharma partner, you'll be able to extend and deepen on the knowledge and understanding of cellular oncogenic pathways and immune system function, to advance on research across Oncology and Inflammation & Autoimmunity.


What you will be doing:

  • Supports and executes the data review activities, including data validation and analytics, that contribute to delivery of clinical data that meets agreed upon data integrity standards.

  • Supports activities related to development of the clinical data management systems (CDMS), as needed.

  • Supports and executes the data review activities, including data validation and analytics, associated with a clinical trial to ensure the end product of clinical data meets agreed upon data integrity standards.

  • Detects risks and signals in the data using quality indicators.

  • Performs root cause analysis of detected data issues.

  • Reviews clinical and third party data for subjects enrolled in clinical research protocols based on edit specifications/ Integrated data review plan to facilitate data review.

  • Maintains clinical data management related study documentation as appropriate.

  • Manages third party data reconciliation and data review process.

  • Ensures study and task metrics are tracked and communicated to the clinical data scientist, project team and functional management.

  • Responsible for review of standard quality indicator review including root cause analysis for identification of underlying


You are:

  • Bachelor’s degree in Science or Health

  • 4 years of relevant experience in Clinical Data Management

  • Advanced English

  • Previous experience in Oncology



Why 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.

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.

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, colour, 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.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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