This dual role involves overseeing the performance and development of CRAs while managing vendor relationships to ensure quality monitoring
Job Summary
This dual role involves overseeing the performance and development of CRAs while managing vendor relationships to ensure quality monitoring.
The ideal candidate must have a strong background in clinical research with excellent leadership capabilities to manage multiple responsibilities effectively.
Candidates are expected to support clinical development audits and ensure CAPA follow-up implementation for all site inspections.
Matching Summary
Match Score: 75
This dual role involves overseeing the performance and development of CRAs while managing vendor relationships to ensure quality monitoring.
Skills & Requirements
Must-have
7 years clinical research experience
GCP/ICH regulatory compliance knowledge
CRA performance management skills
Vendor relationship oversight
Site audit and inspection support
Nice-to-have
Advanced degree in health sciences
Digital tool proficiency
Conflict resolution capabilities
Diversity and inclusion commitment
Key Requirements
Minimum 7 years experience in clinical trials
Degree in scientific or health discipline
Thorough understanding of GCP/ICH standards
Work Rights
Relocation not supported; location must be accessible