Senior Clinical Research Scientist

hace 3 semanas


Madrid, Madrid, España Mygwork A tiempo completo

About the Role:

This position at ICON plc involves working as a Senior Clinical Research Scientist within the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence.

Responsibilities:

  • Develop a medical data review plan to determine data retrieval strategies for MRP/protocol.
  • Create a study-specific Table of Contents (TOC) if needed, including core TFLs and compound-specific TFLs.
  • Review Safety TFLs at a specified frequency as outlined in the data review plan.
  • Develop a Safety Slide Deck (SSD) for cross-functional review, focusing on adverse events, treatment emergent serious adverse events, and other key safety findings.
  • Query identifiable safety-related medical discrepancies or requests for clarification in the appropriate ED C.
  • Prepare a summary of the safety data review, including data reviewed, safety findings observed, and data cleaning requests/observations.
  • Perform additional data review or compilation as needed.
  • Review patient-specific and overall safety data presented in the clinical study report (CSR).
  • Prepare medical protocol deviations for cross-functional review.

About ICON:

We're committed to building a diverse culture that rewards high performance and nurtures talent. Our benefits are designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.

At ICON, diversity, inclusion, and belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates.



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