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gcp cross-functional collaboration clinical research site management imagingπ 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.
π― 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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