Clinical Trials Specialist

hace 7 horas

Madrid, Madrid, España Iqvia A tiempo completo
Job Description

As a Clinical Trials Specialist at IQVIA, you will be responsible for ensuring the quality and integrity of clinical trials data. This includes validating connected devices, such as medical devices that collect health data from trial participants, and ensuring that they meet the required standards.

Key Responsibilities
  • Validate connected devices to ensure they meet the required standards
  • Review business requirements and create test cases to ensure that devices are functioning correctly
  • Execute UAT (User Acceptance Testing) to ensure that devices are meeting the required standards
  • Create site and subject-facing documentation, such as Investigator Manuals and Patient Facing Guides
  • Project manage the onboarding and operationalizing of connected devices solutions
  • Provide support to sites through troubleshooting, problem identification, solution identification, and resolution
  • Coordinate the routing and handling of Requests for Change to the next level of support under broad supervision
  • Escalate issues relating to product support or product operations to the next level of support
  • Work closely with various inter-departments to ensure faster resolution and solution implementation
  • Provide feedback based on client experiences to product and professional services teams for product and process improvements
Qualifications
  • Bachelor's Degree in Computer Science, a related field, or equivalent experience
  • Understanding of clinical trials is required
  • Experience with clinical research and eSource platform is preferred
  • Experience with connected devices and data management of connected devices is preferred

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