Clinical Trial Monitoring Manager
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Job Summary
Leading the clinical trial monitoring program for a diverse portfolio of studies, the full-time Clinical Trial Monitoring Manager will oversee compliance with protocols and regulations, supervise monitoring personnel, and manage vendor relationships in a remote environment.
Key responsibilities:
- Oversee the development and management of clinical research protocols, ensuring compliance with regulatory requirements
- Collaborate with Principal Investigators and research teams to ensure adherence to study protocols and GCP guidelines
- Supervise monitoring personnel, manage performance metrics, and review monitoring plans and reports
Required qualifications:
- Bachelor's degree in a relevant area
- Minimum of 6 years of progressive experience in clinical research operations, including management experience
- Significant experience with regulatory compliance and Good Clinical Practice guidelines
- Proven ability to lead projects and teams through change and improve processes
- Experience with clinical data management processes and systems
Complete Job Description
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