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gcp cross-functional collaboration clinical research site management imaging

πŸ“‹ Description

  • Serve as primary liaison between sponsor and sites; ensure effective communication.
  • Support sites in meeting patient recruitment goals with guidance on strategies.
  • Monitor site performance; address protocol, recruitment, and data concerns.
  • Ensure site staff training and compliance with study protocols, GCP, and regs.
  • Collaborate with site staff to overcome recruitment barriers; track metrics.
  • Conduct regular site visits (remote/in-person) to provide hands-on support.

🎯 Requirements

  • Bachelor's degree in healthcare-related field.
  • Minimum 3 years of clinical research, focused on site management and patient recruitment.
  • Strong knowledge of clinical trial protocols, GCP guidelines, and regulatory requirements.
  • Proven ability to work independently and manage multiple clinical sites simultaneously.
  • Flexibility to travel up to 50% for site visits and meetings.
  • Advanced degree in nursing, clinical research, or related field (preferred).
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