Clinical Trials Coordinator

hace 1 mes


Barcelona, Barcelona, España Creal A tiempo completo
Job Title: Quality Management Coordinator

At Creal, we are seeking a highly skilled Quality Management Coordinator to join our team. This is a unique opportunity to contribute to the development and implementation of quality management systems in clinical trials.

Key Responsibilities:
  • Develop and maintain Standard Operating Procedures (SOPs) for clinical trials.
  • Coordinate the review and approval process of SOPs.
  • Organize and track internal training on SOPs.
  • Maintain an internal registry of clinical trials conducted by ISGlobal researchers.
  • Ensure compliance with regulatory requirements and ethics committee submissions.
  • Support researchers in clinical trials registration and annual re-approvals.
  • Verify proper archiving of projects and coordinate internal audits.
  • Prepare information for reporting clinical trials activity.
Requirements:
  • Master's degree in health sciences or related field.
  • Minimum 5 years of experience in managing clinical trials.
  • Knowledge of regulatory agencies and ethics committee submissions.
  • Experience in quality management and clinical research.

As a Quality Management Coordinator, you will play a critical role in ensuring the quality and integrity of clinical trials. If you have a passion for quality management and clinical research, we encourage you to apply for this exciting opportunity.



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